3-(Methylsulphonyl)aniline → HCID 68436084, compound

HRID 1170128Notes

Reaction equation

HRID 1170128 reaction equation
I[C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][C:6](Cl)=[N:7]2.[CH3:13][C:14]1[O:18][C:17]([CH2:19][NH2:20])=[CH:16][CH:15]=1.[CH3:21][S:22]([C:25]1[CH:26]=[C:27]([CH:29]=[CH:30][CH:31]=1)[NH2:28])(=[O:24])=[O:23]>>[CH3:21][S:22]([C:25]1[CH:26]=[C:27]([NH:28][C:2]2[C:3]3[CH:4]=[CH:5][C:6]([NH:20][CH2:19][C:17]4[O:18][C:14]([CH3:13])=[CH:15][CH:16]=4)=[N:7][C:8]=3[CH:9]=[CH:10][CH:11]=2)[CH:29]=[CH:30][CH:31]=1)(=[O:23])=[O:24]

Participants

4

Reactant 3

HCID 4280293-(Methylsulphonyl)anilineHCID 27246835-Methyl-2-furylmethylamineHCID 457894242-Chloro-5-iodoquinoline

Product 1

HCID 68436084HCID 68436084, compound

Procedure

The title compound, MS: m/e=408.4 (M+H+), was prepared in accordance with the general method of example 1 from 5-iodo-2-chloroquinoline (CAS 455955-26-7), 5-methyl-2-furanmethanamine and 3-methylsulfonylaniline.

Sources & evidence

ORD record
ord-c87682f90fbe4624a024fbb4388341b8
Source dataset
uspto-grants-2010_11
Patent number
US07825253B2

Reaction notes

Loading…