4-(Bromomethyl)pyridine → HCID 57658785, compound
Reaction equation
Br[CH2:2][C:3]1[CH:8]=[CH:7][N:6]=[CH:5][CH:4]=1.C([O:11][C:12](=[O:30])[CH2:13][O:14][C:15]1[CH:20]=[CH:19][C:18]([Br:21])=[CH:17][C:16]=1/[CH:22]=[C:23]1/[C:24](=[O:29])[NH:25][C:26](=[O:28])[S:27]/1)C>>[Br:21][C:18]1[CH:19]=[CH:20][C:15]([O:14][CH2:13][C:12]([OH:30])=[O:11])=[C:16]([CH2:22][CH:23]2[S:27][C:26](=[O:28])[N:25]([CH2:2][C:3]3[CH:8]=[CH:7][N:6]=[CH:5][CH:4]=3)[C:24]2=[O:29])[CH:17]=1Participants
3
Procedure
Prepared from 4-bromomethylpyridine and 4-bromo-2-[2,4-dioxothiazolidin-(5Z)-ylidenemethyl]phenoxyacetic acid ethyl ester according to GP13, GP14 and GP16: LC/MS (an10p8): Rt 2.1 min, m/z 451 [M+H]+.
Sources & evidence
- ORD record
- ord-4968043ba37c478981d74d4f20306224
- Source dataset
- uspto-grants-2011_09
- Patent number
- US08022063B2
Reaction notes
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