Bromoacetyl bromide → HCID 10050739, compound

HRID 2115358Notes

Reaction equation

HRID 2115358 reaction equation
Br[CH2:2][C:3](Br)=[O:4].[CH:6]1([CH2:9][NH:10][CH2:11][CH2:12][CH3:13])[CH2:8][CH2:7]1.[NH2:14][C:15]1[CH:16]=[CH:17][C:18]([Cl:21])=[N:19][CH:20]=1.[C:22]([C:26]1[CH:31]=[CH:30][C:29]([S:32](Cl)(=[O:34])=[O:33])=[CH:28][CH:27]=1)([CH3:25])([CH3:24])[CH3:23]>>[C:22]([C:26]1[CH:31]=[CH:30][C:29]([S:32]([N:14]([C:15]2[CH:20]=[N:19][C:18]([Cl:21])=[CH:17][CH:16]=2)[CH2:2][C:3]([N:10]([CH2:9][CH:6]2[CH2:8][CH2:7]2)[CH2:11][CH2:12][CH3:13])=[O:4])(=[O:34])=[O:33])=[CH:28][CH:27]=1)([CH3:25])([CH3:23])[CH3:24]

Participants

5

Reactant 4

HCID 61147Bromoacetyl bromideHCID 793055-Amino-2-chloropyridineHCID 117787Cyclopropanemethanamine, N-propyl-HCID 1398824-t-Butylbenzenesulfonyl chloride

Product 1

HCID 10050739HCID 10050739, compound

Procedure

prepared by reaction of 2-bromoacetyl bromide with N-cyclopropylmethyl-N-propylamine, 5-amino-2-chloropyridine and 4-tert-butyl-benzenesulfonyl chloride

Sources & evidence

ORD record
ord-2bbbefd76345487db519779eb152a5ba
Source dataset
uspto-grants-2008_10
Patent number
US07435815B2

Reaction notes

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