HCID 20558007, compound → HCID 178428582, compound

HRID 1660144Notes

Reaction equation

HRID 1660144 reaction equation
[NH:1]([C:5]1[S:6][CH:7]=[C:8]([CH2:10][S:11][CH2:12][CH2:13][NH2:14])[N:9]=1)[C:2]([NH2:4])=[NH:3].CS[C:17]1[NH:18][CH2:19][C:20]([CH3:27])([CH3:26])[CH2:21][C:22]=1[N+:23]([O-:25])=[O:24]>>[NH:1]([C:5]1[S:6][CH:7]=[C:8]([CH2:10][S:11][CH2:12][CH2:13][NH:14][C:17]2[NH:18][CH2:19][C:20]([CH3:27])([CH3:26])[CH2:21][C:22]=2[N+:23]([O-:25])=[O:24])[N:9]=1)[C:2]([NH2:4])=[NH:3]

Participants

3

Reactant 2

HCID 20558007HCID 20558007, compoundHCID 1785127232-[4-(2-Aminoethylsulfanylmethyl)-1,3-thiazol-2-yl]guanidine

Product 1

HCID 178428582HCID 178428582, compound

Procedure

The title compound is prepared from 2-(2-guanidino-4-thiazolylmethylthio)ethylamine and 2-methylthio-3-nitro-5,5-dimethyl-1,4,5,6-tetrahydropyridine by a process analogous to that of Example 1.

Sources & evidence

ORD record
ord-54696732a23a49068e4325ce64381d47
Source dataset
uspto-grants-1981_12
Patent number
US04307104

Reaction notes

Loading…