P-Anisidine → HCID 10388105, compound

HRID 2115349Notes

Reaction equation

HRID 2115349 reaction equation
Br[CH2:2][C:3](Br)=[O:4].[CH2:6]([NH:8][CH2:9][CH3:10])[CH3:7].[CH3:11][O:12][C:13]1[CH:18]=[CH:17][C:16]([NH2:19])=[CH:15][CH:14]=1.[C:20]([C:24]1[CH:29]=[CH:28][C:27]([S:30](Cl)(=[O:32])=[O:31])=[CH:26][CH:25]=1)([CH3:23])([CH3:22])[CH3:21]>>[C:20]([C:24]1[CH:29]=[CH:28][C:27]([S:30]([N:19]([C:16]2[CH:17]=[CH:18][C:13]([O:12][CH3:11])=[CH:14][CH:15]=2)[CH2:2][C:3]([N:8]([CH2:9][CH3:10])[CH2:6][CH3:7])=[O:4])(=[O:32])=[O:31])=[CH:26][CH:25]=1)([CH3:23])([CH3:21])[CH3:22]

Participants

5

Procedure

prepared by reaction of 2-bromoacetyl bromide with diethylamine, p-anisidine and 4-tert-butyl-benzenesulfonyl chloride

Sources & evidence

ORD record
ord-6fde65b667c44573bb61b3ed9a0bb55c
Source dataset
uspto-grants-2008_10
Patent number
US07435815B2

Reaction notes

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