N-Methylcyclopropanamine → Imidazole-1-sulfonic acid cyclopropyl-methyl-amide

HRID 1928782Notes

Reaction equation

[CH:1]1([NH:4][CH3:5])[CH2:3][CH2:2]1.FC(F)(F)S([O-])(=O)=O.[N:14]1([S:19](N2C=C[NH+](C)C2)(=[O:21])=[O:20])[CH:18]=[CH:17][N:16]=[CH:15]1>>[CH:1]1([N:4]([CH3:5])[S:19]([N:14]2[CH:18]=[CH:17][N:16]=[CH:15]2)(=[O:21])=[O:20])[CH2:3][CH2:2]1

Participants

Reactant 2

HCID 11029756N-Methylcyclopropanamine

HCID 866341663-(1H-Imidazol-1-ylsulfonyl)-1-methyl-1H-imidazolium trifluoromethanesulfonate

Product 1

HCID 68915335Imidazole-1-sulfonic acid cyclopropyl-methyl-amide

Procedure

Imidazole-1-sulfonic acid cyclopropyl-methyl-amide was prepared in accordance with step A of the general method described in example 76 from cyclopropyl-methylamine and 3-(1H-imidazol-1-ylsulfonyl)-1-methyl-1H-imidazolium trifluoromethanesulfonate; MS: m/e=202.5 (M+H+).

Sources & evidence

ORD record: ord-a4c1a4587af84e509033e4e9fa33732f
Source dataset: uspto-grants-2012_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08183380B2

Reaction notes

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