Carbonochloridic acid, cyclohexyl ester → HCID 140411176, compound

HRID 1954375Notes

Reaction equation

HRID 1954375 reaction equation
[CH3:1][N:2]1[C:6]2[CH:7]=[CH:8][C:9]([N:11]([S:17]([C:20]3[CH:21]=[CH:22][CH:23]=[C:24]4[C:29]=3[N:28]=[CH:27][CH:26]=[CH:25]4)(=[O:19])=[O:18])[CH2:12][C:13]([O:15][CH3:16])=[O:14])=[CH:10][C:5]=2[N:4]=[C:3]1[CH2:30][O:31][C:32]1[CH:37]=[CH:36][C:35]([C:38](=[NH:40])[NH2:39])=[CH:34][CH:33]=1.Cl[C:42]([O:44][CH:45]1[CH2:50][CH2:49][CH2:48][CH2:47][CH2:46]1)=[O:43]>>[CH3:1][N:2]1[C:6]2[CH:7]=[CH:8][C:9]([N:11]([S:17]([C:20]3[CH:21]=[CH:22][CH:23]=[C:24]4[C:29]=3[N:28]=[CH:27][CH:26]=[CH:25]4)(=[O:19])=[O:18])[CH2:12][C:13]([O:15][CH3:16])=[O:14])=[CH:10][C:5]=2[N:4]=[C:3]1[CH2:30][O:31][C:32]1[CH:33]=[CH:34][C:35]([C:38](=[NH:39])[NH:40][C:42]([O:44][CH:45]2[CH2:50][CH2:49][CH2:48][CH2:47][CH2:46]2)=[O:43])=[CH:36][CH:37]=1

Participants

3

Reactant 2

HCID 83262Carbonochloridic acid, cyclohexyl esterHCID 53825809HCID 53825809, compound

Product 1

HCID 140411176HCID 140411176, compound

Procedure

Prepared analogously to Example 31 from 1-methyl-2-[(4-amidino-phenyl)-oxymethyl]-5-[N-(methoxycarbonylmethyl)-quinoline-8-sulphonylamino)-benzimidazole and cyclohexyl chloroformate.

Sources & evidence

ORD record
ord-c4688dda073b4728820658b56b6b2a26
Source dataset
uspto-grants-2000_09
Patent number
US06121308

Reaction notes

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