US 5,017,599 AGrant
Site Specific Alkylating Agents
Issue Date:1991-05-21
•5 Claims
Abstract
The invention relates to distamycin A analogs of the following formula ##STR1## wherein n is 2, 3 or 4; A is an optionally substituted divalent radical chosen from ##STR2## and -Het- wherein Het is a pentatomic or hexatomic heteromonocyclic ring, except pyrrole; and wherein either one of R.sub.1 and R.sub.2 is hydrogen and the other is an acylating moiety or R.sub.1 and R.sub.2 are both hydrogen or both alkyl groups optionally substituted, including the pharmaceutically acceptable salts of the said compounds. The compounds of the invention can be useful antitumor and antiviral agents.
Metadata
Assignee
- Farmitalia Carlo Erba, SpA
Inventors
- Ettore Lazzari
- Federico Arcamone
- Sergio Penco
- Maria A. Verini
- Nicola Mongelli
Application Information
Application Number:US 4858476
Filing Date:1990-02-21
Priority Date:1987-05-15
Art Unit:187
Classifications
IPC:
C07D20714A61K 3140
Field of Search:
548514518422
Patent Drawings
This patent does not have any drawings.
Description
EXAMPLE 1
.beta.-[1-methyl-4-[1-methyl-4-[1-methyl-4-[-(N'-methyl-N'-nitrosoureidoben zene)-1-carboxamido]pyrrole-2-carboxamido]pyrrole-2-carboxamido]pyrrole-2-c arboxamido]propionamidine, hydrochloride
A solution of 0.1 ml of triethylamine in 1 ml of DMF was added in 5' to a stirred solution of 0.41 g of N-deformyl distamycin in 2.5 ml of DMF at room temperature and under nitrogen. After 15' 0.17 g of 4-(N-nitroso-N-methylureido)benzoic acid and 0.16 g of dicyclohexylcarbodiimide were added in small portions. The reaction mixture was stirred two hours and 25 ml of ethyl ether were added. The solid collected by filtration was purified by chromatography on silica gel with mixtures of ethylacetate, methanol and acetic acid, yielding 0.175 g of the title compound, m.p. 205-210.degree. C. (dec.) (from isopropanol).
FD-MS: m/z 572 [6, (M-C.sub.2 H.sub.2 N.sub.2 O.sub.2).sup.+. ]; 555 [7.5, (M-NH.sub.3 -C.sub.2 H.sub.2 N.sub.2 O.sub.2).sup.+. ];502 (100);
PMR (DMSO-d.sub.6).delta.: 10.90 (broad signal, 1H); 10.31 (s, 1H); 9.99, 9.92 (s, 2H); 8.97, 8.63 (broad signal, 4H); 8.22 (t, J=5.5Hz, 1H); 7.97, 7.86 (two doublets, J=8.8Hz, 4H); 7.32, 7.24, 7.18, 7.11, 7.06, 6.94 (broad signal, 6H); 3.86, 3.83, 3.80 (s; 9H); 3.48 (m, 2H); 3.17 (s, 3H); 2.60 (m, 2H).
By analogous procedure it can be also prepared the corresponding N'-(2-chloro-ethyl)-N'-nitrosoureido benzoyl derivative of N-deformyldistamycin, i.e. the compound .beta.-[1-methyl-4-[-methyl-4-[1-methyl-4-[1-methyl-4-[4-(N'-(2-chloro-eth yl-N'-nitrosoureido-benzene)-1-carboxamido]pyrrole-2-carboxamido]pyrrole-2- carboxamido]pyrrole-2-carboxamido]propionamidine, hydrochloride. m.p. 182.degree. C. (dec.),
MS-FD : M.sup.+ (707);M.sup.+ -17 (690);M.sup.30 -70 (637)
PMR (DMSO-d.sub.6).delta.: 2.39 (t,2H); 3.50 (dt,2H); 3.69 (t,2H) 3.79 (s,3H); 3.85 (s,3H); 3.89 (s,3H); 4.19 (t,2H); 6.89-7.25 (m,8H); 7.88 (m,2H); 9.01 (b,4H); 9.92 (s,1H); 9.94 (s,1H); 10.06 (s1H).
UV (EtOH 95%;C=0.00172%): ##STR19##
EXAMPLE 2
.beta.[1 methyl-4-[1-methyl-4-[1-methyl 4-(4-N,N-bis(2-chloroethyl)aminothiophen-2-carboxamido]pyrrole-2-carboxami do]pyrrole-2-carboxamido]pyrrole-2-carboxamido]propionamidine, hydrochloride
Step One
The intermediate 4-[N,N-bis-(2-chloroethyl)]-aminothiophen-2-carboxylic acid.
Starting from 1.74 g of methyl-4-nitrothiophen-2-carboxylate, by reduction with zinc :n methanol solution saturated with hydrogen chloride [according to Can. J. Chem. 44, 2888 (1966) for the reduction of the 5-nitrothiophen derivative] 0.90 g of methyl-4-aminothiophen-2-carboxylate were obtained, m.p. 81-82.degree. C. (from diisopropylether).
4 g of cold ethylene oxide were introduced to a solution of 0.9 g of methyl-4-aminothiophen-2-carboxylate in 12.5 ml of 40% aqueous acetic acid at 5.degree. under stirring. The mixture maintained overnight at room temperature in a sealed flask was concentrated to small volume and then diluted with 25 ml of water. Solid sodium bicarbonate was added and the mixture was extracted with ethyl acetate. By evaporation of the organic solvent 1.3 g of methyl-4-[N-N-bis-(2-hydroxyethyl)]-aminothiophen-2-carboxylate were obtained as a light brown oil which solidifies on standing, m.p. 68-60.degree. C. (from ethylacetate-hexane 60/40).
The bis-hydroxyethylamino derivative obtained (1.3 g) was dissolved in 1.96 ml of phosphorous oxychloride and the mixture was refluxed 45 minutes. After evaporation under vacuum the dark residue was treated with 7.75 ml of concentrated hydrochloric acid at 100.degree. for three hours. The mixture was cooled, 21 ml of cold water were added and the resulting solution was extracted with ethyl acetate. Evaporation of the organic solvent and purification of the solid residue by chromatography on a silica gel column eluting with a mixture of ethyl acetate-methanol afforded 0.49 g of 4-[N,N-bis(2-chloroethyl)]-aminothiophen-2-carboxylic acid, m.p. 135-137.degree. C. (from benzene-hexane 60/40);
EI/MS: m/z 267 (11,M.sup.+); 218 (100); 63 (57); PMR (CDCl.sub.3) .delta.: 9.50 (broad signal, 1H); 7.45(d, J=2.3Hz, 1H); 6.30 (d, J=2.3Hz, 1H); 3.63 (s, 8H).
Step two
The title compound.
A solution of 0.1 ml of triethylamine in 0.5 ml of DMF was added to a solution of 0.45 g of deformyl distamycin dihydrochloride in 4.5 ml of DMF at room temperature and under nitrogen. The mixture was treated with 0.23 g of 4-[N,N-bis-(2-chloroethyl)]-aminothiophen-2-carboxylic acid and 0.77 g of dicyclohexylcarbodiimide in small portions. The resulting mixture was stirred overnight, then filtered and evaporated to dryness under vacuum. The solid residue was purified by chromatography on silica gel column eluting with mixtures of ethyl acetate and ethanol (9:1 and 8:2 by volume). 0.22 g of the title compound were obtained m.p.199-204.degree. C. (after recrystallization from isopropyl alcohol); FD-MS: m/z 703 MH.sup.+ ; PMR (DMSO-d.sub.6).delta.: 10.28 (broad signal, 1H); 9.94, 0.98 (s, 2H); 8.9-9.3 (broad signal, 4H); 8.24 (t, J=5.5Hz, 1H); 7.67, 6.44 (two doublets, J=1.6Hz, 2H); 7.24, 7.18, 7.07, 7.04, 6.92 (d, J=1.8Hz, 6H); 3.85, 3.83, 3.79 (s, 9H); 3.8-3.6 (m, 8H); 3.47 (m, 2H); 2.57 (m, 2H).
By analogous procedure the following compounds can be prepared: .beta.-[1-methyl-4-[1-methyl-4-[1-methyl-4-[-4-[N,N -bis(2-chloroethyl)]aminoimidazole-1-methyl-2-carboxamido]pyrrole-2-carbox amido]pyrrole-2-carboxamido]pyrrole-2-carboxamido]propionamidine hydrochloride;
.beta.-[1-methyl-4-[1-methyl-4-[1-methyl-4-[5-[N,N-bis-(2-chloroethyl)]-ami noimidazole-1-methyl-2-carboxamido]pyrrole-2-carboxamido]pyrrole-2-carboxAm ido]pyrrole-2-carboxamido]propionamidine hydrochloride;
.beta.-[1-methyl-4-[1-methyl-4-[1-methyl-4-[4-(N,N-bis(2-chloroethyl) aminothiazole-2-carboxamido]pyrrole-2-carboxamido]pyrrole-2-carboxamido]py rrole-2-carboxamido]propionamidine hydrochloride;
.beta.-[1-methyl-4-[-1-methyl-4-[1-methyl-4-[5-[N,N-bis(2-chloroethyl) aminothiazole-2-carboxamido]pyrrole-2-carboxamido]pyrrole-2-carboxamido]py rrole-2-carboxamido]propionamidine hydrocloride.
EXAMPLE 3
.beta.-[1-methyl-4-[1-methyl-4-[1-methyl-4-(4-N,N-bis(2-chloroethylamino benzene-1-carboxamido]pyrrole-2-carboxamido]pyrrole-2-carboxamido]pyrrole- 2-carboxamido]propionamidine. hydrochloride
A solution of 0.195 g of sodium bicarbonate in 3 ml of water was added to a cooled solution of 0.4 g of deformyl distamycin in 21 ml of ethanol. To this mixture a solution of 0.32 g of 4-N,N-(2-chloroethyl)aminobenzoyl chloride in 3 ml of benzene was added dropwise. The mixture was stirred three hours at 5.degree. and then twelve hours at room temperature. Evaporation under vacuum gave a solid residue which was chromatographed on silica gel column eluting with mixtures of chloroform-methanol (9:1 and 7:3 by volume) yielding 0.22 g of the title compound, m.p.295.degree. C dec. (from isopropyl alcohol and ethyl ether; FD-MS: m/z 697 (34, MH.sup.30); 679 (100, M-NH.sub.3);
PMR (DMSO-d.sub.6).delta.: T=50.degree. C.; 9.91 (s, 1H); 9.82, 9.79 (s, 2H); 8.94, 8.61 (broad signal, 4H); 8.11 (t, J=5.5Hz, 1H); 7.85, 6.82 (two doublets, J=8.9Hz. 4; 7.26, 7.20, 7.15, 7.07, 7.05. 6.94 (d, J=1.6Hz, 6H); 3.85, 3.84, 3.81 (s; 9H); 3,78 (s, 8H); 3.51 (m, 2H); 2.64 (t, J=6.6Hz, 2H).
By analogous procedure the following compounds can be obtained:
.beta.[1-methyl-4-[1-methyl-4-[1-methyl-4-[3-N,N-bis(2-chloroethyl) amino-benzene-1-carboxamido]pyrrole-2-carboxamido]pyrrole-2-carboxamido]py rrole-2-carboxamido]propionamidine hydrochloride, m.p. 170.degree. C. (dec.);
MS-FD: M.sup.+ -17 (679); M.sup.30 -70 (626); M.sup.+ -2 (CH.sub.2 CH.sub.2 Cl) (571);
PMR (DMSO-d.sub.6) .delta.:2.63 (t,3H); 3.35-4.00 (m,19H); 6.80-7.40 (m,10H); 8.20 (t,1H); 8.88 (b,4H); 9.90 (1.1H); 9.94 (s,1H); 10.15 (s,1H).
UV (EtOH 95%: C=0.003107%):
.beta.-[1-methyl-4-[1-methyl-4-[1-methyl-4-[4-oxiranecarbonyl-amino-benzene -1-carboxamido]pyrrole-2-carboxamido]pyrrole-2-carboxamido]pyrrole-2-carbox amido]propionamidine hydrochloride;
.beta.-[1-methyl-4-[1-methyl-4-[1-methyl-4-[3--oxiranecarbonylamino-benzene -1-carboxamido]pyrrole-2-carboxamido]-pyrrole-2 -carboxamido]pyrrole-2-carboxamido]propionamidine hydrochloride;
.beta.-[1-methyl-4-[1 methyl-4-[1-methyl-4-[4-[1-(aziridine) carbonylamino-benzene-1-carboxamido]pyrrole-2-carboxamido]pyrrole-2-carbox amido]pyrrole-2-carboxamido]propionamidine hydrochloride;
.beta.-[1-methyl-4-[1-methyl-4-[1-methyl-4-[3-[1-(aziridine) carbonylamino-benzene-1-carboxamido]pyrrole-2-carboxamido]pyrrole-2-carbox amido]pyrrole-2-carboxamido]-propionamidine hydrochloride.
EXAMPLE 4
Tablets each weighing 0.250 g and containing 50 mg of the active substance can be manufactured as follows: Composition (for 10,000 tablets)
.beta.[1-methyl-4-[1-methyl-4-[1-methyl-4[4-N,N-bis(2-chloroethyl)amino-ben zene-1-carboxamodo]pyrrole-2-carboxamido]pyrrole-2-carboxamido]pyrrole-2-ca rboxamido]propionamidine hydrochloride: 500 g
Lactose: 1,400 g
Corn starch: 500 g
Talc powder: 80 g
Magnesium stearate: 20 g.
The .beta.-[1-methyl-4-[1-methyl-4[1-methyl-4-[4-N,N-bis(2-chloroethyl) amino-benzene-1-carboxamido]pyrrole-2-carboxamido]pyrrole-2-carboxamido]py rrole-2-carboxamido]propionamidine hydrochloride, the lactose and half the corn starch are mixed: the mixture is then forced through a sieve of 0.5 mm mesh size. Corn starch (10 g) is suspended in warm water (90 ml) and the resulting paste is used to granulate the powder. The granulate is dried, comminuted on a sieve of 1.4 mm mesh size, then the remaining quantity of starch, talc and magnesium stearate is added, carefully mixed and processed into tablets.
EXAMPLE 5
Capsules, each dosed at 0.200 g and containing 20 mg of the active substance can be prepared as follows: Composition for 500 capsules:
.beta.-[1-methyl-4-[1-methyl-4-[1-methyl-4-[4-N,N-bis(2-chloroethyl) amino-benzene-1-carboxamido]pyrrole-2-carboxamido]pyrrole-2-carboxamido]py rrole-2-carboxamido]propionamidine hydrochloride: 10 g
Lactose: 80 g
Corn starch: 5 g
Magnesium stearate: 5 g. This formulation can be encapsulated in two-piece hard gelatin capsules and dosed at 0.200 g for each capsule.
EXAMPLE 6
Intramuscular injection 25 mg/ml
An injectable pharmaceutical composition can be manufactured by dissolving 25 g of .beta.[1-methyl-4-[1-methyl-4-[1-methyl-4[4-N,N-bis(2-chloro-ethyl-)aminot hiophen-2-carboxamido]pyrrole-2-carboxamiso]pyrrole-2-carboxamido]pyrrole-2 -carboxamido]propionamidine hydrochloride in sterile propyleneglycol (1000 ml) and sealing ampoules of 1-5 ml.
Claims
We claim:
1. .beta.-[1-methyl-4-[1-methyl-4-[1-methyl-4-4-[N,N-bis(2-chloroethyl) amino-benzene-1-carboxamido]pyrrole-2-carboxamido]pyrrole-2-carboxamido]py rrole-2-carboxamido]propionamidine, and the pharmaceutically acceptable salts thereof.
2. Compound of claim 1, wherein said compound is in the form of the hydrochloride salt.
3. A pharmaceutical composition for producing an antitumor or antiviral effect containing, as an active principle, an antitumor-effective amount or an antiviral-effective amount of the compound of claim 1, or a pharmaceutical acceptable salt thereof, and a pharmaceutical acceptable carrier and/or diluent.
4. A method of producing an antitumor effect in a patient in need of such effect, said method comprising administering to said patient an antitumor effective amount of a compound of claim 1.
5. A method of producing an antiviral effect in a patient in need of such effect, said method comprising administering to said patient an antiviral-effective amount of a compound of claim 1.
Patent Citations (9)
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- Chemical Abstracts: 68:21767z, 68:21768a, 88:83397a, 88:201h, 97:215877e, 82:25984e, 99:176269c, 95:61898g, 89:102109x, 81:163162r, 100:39669h.
- Chemical Abstracts: 84:150434t, 90:87174g, 88:50585q, 68:87088k; 71:101629h, 71:101631c, 79:38445t, 77:14824y, 76:108639y, and 76:149456e.