HCID 13646629, compound → HCID 178430892, compound

HRID 2198745Notes

Reaction equation

HRID 2198745 reaction equation
Cl.Cl.[NH:3]([C:7]1[S:8][CH:9]=[C:10]([CH2:12][S:13][CH2:14][CH2:15][NH2:16])[N:11]=1)[C:4]([NH2:6])=[NH:5].CS([C:20]1[NH:21][CH:22]=[C:23]([CH3:28])[C:24]=1[N+:25]([O-:27])=[O:26])=O>>[NH:3]([C:7]1[S:8][CH:9]=[C:10]([CH2:12][S:13][CH2:14][CH2:15][NH:16][C:20]2[NH:21][CH:22]=[C:23]([CH3:28])[C:24]=2[N+:25]([O-:27])=[O:26])[N:11]=1)[C:4]([NH2:6])=[NH:5]

Participants

3

Reactant 2

HCID 13646629HCID 13646629, compoundHCID 178478806HCID 178478806, compound

Product 1

HCID 178430892HCID 178430892, compound

Procedure

The title compound is prepared from 2-(2-Guanidino-4-thiazolylmethylthio)-ethylamine dihydrochloride and 2-methylsulphinyl-4-methyl-3-nitropyrrole by a process analogous to that described in Example 1.

Sources & evidence

ORD record
ord-816c36066b2f4109bc96aa1a233d4f4c
Source dataset
uspto-grants-1982_11
Patent number
US04359466

Reaction notes

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