HCID 20558008, compound → HCID 178512703, compound

HRID 1660145Notes

Reaction equation

HRID 1660145 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][CH:20]([CH2:26][CH2:27][C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[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][CH:20]([CH2:26][CH2:27][C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=3)[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 20558008HCID 20558008, compoundHCID 1785127232-[4-(2-Aminoethylsulfanylmethyl)-1,3-thiazol-2-yl]guanidine

Product 1

HCID 178512703HCID 178512703, compound

Procedure

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

Sources & evidence

ORD record
ord-2a717bdd75a2430cbd7e7fe90c324842
Source dataset
uspto-grants-1981_12
Patent number
US04307104

Reaction notes

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