Dimethylsulphamoyl chloride → HCID 44217996, compound

HRID 1669714Notes

Reaction equation

[CH3:1][C:2]1[O:6][C:5]([CH2:7][NH:8][C:9]2[CH:18]=[CH:17][C:16]3[C:15]([NH2:19])=[CH:14][CH:13]=[CH:12][C:11]=3[N:10]=2)=[CH:4][CH:3]=1.[CH3:20][N:21]([CH3:26])[S:22](Cl)(=[O:24])=[O:23]>>[CH3:20][N:21]([CH3:26])[S:22]([NH:19][C:15]1[CH:14]=[CH:13][CH:12]=[C:11]2[C:16]=1[CH:17]=[CH:18][C:9]([NH:8][CH2:7][C:5]1[O:6][C:2]([CH3:1])=[CH:3][CH:4]=1)=[N:10]2)(=[O:24])=[O:23]

Participants

Reactant 2

HCID 83372Dimethylsulphamoyl chloride

HCID 44217679HCID 44217679, compound

Product 1

HCID 44217996HCID 44217996, compound

Procedure

The title compound, MS: m/e=361.0 (M+H+), was prepared in accordance with the general method of example 19 from N2-(5-Methyl-furan-2-ylmethyl)-quinoline-2,5-diamine and dimethylsulfamoyl chloride.

Sources & evidence

ORD record: ord-47ecbeaa46e944cca634a58ea59ccb82
Source dataset: uspto-grants-2011_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07989628B2

Reaction notes

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