Diethylamine → HCID 10455780, compound
Reaction equation
Br[CH2:2][C:3](Br)=[O:4].[CH2:6]([NH:8][CH2:9][CH3:10])[CH3:7].[NH2:11][C:12]1[CH:13]=[CH:14][C:15]([Cl:18])=[N:16][CH:17]=1.[C:19]([C:23]1[CH:28]=[CH:27][C:26]([S:29](Cl)(=[O:31])=[O:30])=[CH:25][CH:24]=1)([CH3:22])([CH3:21])[CH3:20]>>[C:19]([C:23]1[CH:28]=[CH:27][C:26]([S:29]([N:11]([C:12]2[CH:17]=[N:16][C:15]([Cl:18])=[CH:14][CH:13]=2)[CH2:2][C:3]([N:8]([CH2:9][CH3:10])[CH2:6][CH3:7])=[O:4])(=[O:31])=[O:30])=[CH:25][CH:24]=1)([CH3:22])([CH3:20])[CH3:21]Participants
5
Procedure
prepared by reaction of 2-bromoacetyl bromide with diethylamine, 5-amino-2-chloropyridine and 4-tert-butyl-benzenesulfonyl chloride
Sources & evidence
- ORD record
- ord-c469b2e42dcf4b4094e30d3b35dd4f7e
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435815B2
Reaction notes
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