Methyl iodide → S-methyl-N-(3-benzoylaminopropyl)dithiocarbamate hydriodide

HRID 1834555Notes

Reaction equation

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

Participants

Reactant 3

HCID 6328Methyl iodide

HCID 6348Carbon Disulfide

HCID 238993n-(3-Aminopropyl)benzamide

Product 1

HCID 86733688S-methyl-N-(3-benzoylaminopropyl)dithiocarbamate hydriodide

Procedure

i. 3-Benzoylaminopropylamine was treated successively with carbon disulphide and methyl iodide according to the general procedure of Example 1(a) (b) to give S-methyl-N-(3-benzoylaminopropyl)dithiocarbamate hydriodide

Sources & evidence

ORD record: ord-9fcf6eb3a61a4acb9ceef6ecb5ec3508
Source dataset: uspto-grants-1978_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04070472

Reaction notes

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