Butanecarbothioyl chloride → HCID 178455545, compound

Reaction equation

[NH2:1][C:2]1[CH:3]=[C:4]([N:8]2[C:12]([SH:13])=[N:11][N:10]=[N:9]2)[CH:5]=[CH:6][CH:7]=1.[CH3:14][CH2:15][CH2:16][C:17](Cl)=[S:18]>>[CH3:14][CH2:15][CH2:16][C:17]([NH:1][C:2]1[CH:3]=[C:4]([N:8]2[C:12]([SH:13])=[N:11][N:10]=[N:9]2)[CH:5]=[CH:6][CH:7]=1)=[S:18]

Participants

Reactant 2

HCID 22343826Butanecarbothioyl chloride

HCID 178507610HCID 178507610, compound

Product 1

HCID 178455545HCID 178455545, compound

Procedure

This compound was prepared from 1-(m-aminophenyl)-5-mercaptotetrazole and 3-methylthiopropionyl chloride [A. Mooradian et al., J. Am. Chem. Soc. 71, 3372 (1949)] according to the same reaction scheme as the one described hereinabove for compound 1.

Workup

custom71, 3372 (1949)] according to the same reaction scheme as the one

Sources & evidence

ORD record: ord-6084609f81af4a169bd01f1ebd4173e0
Source dataset: uspto-grants-1984_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04451555

Reaction notes

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