Cyclohexylamine → HCID 67095879, compound

HRID 2076309Notes

Reaction equation

HRID 2076309 reaction equation
[N+:1]([C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH:6]=[CH:7][C:8](Cl)=[N:9]2)([O-])=O.[F:15][C:16]1[CH:21]=[CH:20][C:19]([S:22](Cl)(=[O:24])=[O:23])=[CH:18][CH:17]=1.[CH:26]1([NH2:32])[CH2:31][CH2:30][CH2:29][CH2:28][CH2:27]1>>[CH:26]1([NH:32][C:8]2[CH:7]=[CH:6][C:5]3[C:10](=[CH:11][CH:12]=[CH:13][C:4]=3[NH:1][S:22]([C:19]3[CH:20]=[CH:21][C:16]([F:15])=[CH:17][CH:18]=3)(=[O:24])=[O:23])[N:9]=2)[CH2:31][CH2:30][CH2:29][CH2:28][CH2:27]1

Participants

4

Reactant 3

HCID 7965CyclohexylamineHCID 95884-Fluorobenzenesulfonyl chlorideHCID 3192512-Chloro-5-nitroquinoline

Product 1

HCID 67095879HCID 67095879, compound

Procedure

The title compound, MS: m/e=400.3 (M+H+), was prepared in accordance with the general method of example 13 from 5-nitro-2-chloroquinoline, 4-fluorobenzenesulfonyl chloride and cyclohexylamine.

Sources & evidence

ORD record
ord-b87287f8f8e442fa839e9591fdd07a5b
Source dataset
uspto-grants-2011_04
Patent number
US07923561B2

Reaction notes

Loading…