Benzeneacetic acid, 4-bromo- → HCID 67479678, compound
Reaction equation
[O:1]1[CH2:6][CH2:5][CH:4]([NH2:7])[CH2:3][CH2:2]1.[Br:8][C:9]1[CH:14]=[CH:13][C:12]([CH2:15][C:16](O)=[O:17])=[CH:11][CH:10]=1>>[Br:8][C:9]1[CH:14]=[CH:13][C:12]([CH2:15][C:16]([NH:7][CH:4]2[CH2:5][CH2:6][O:1][CH2:2][CH2:3]2)=[O:17])=[CH:11][CH:10]=1Participants
3
Procedure
The title compound was prepared in substantially the same way as intermediate (iv) by coupling of tetrahydropyran-4-yl amine with (4-bromo-phenyl)-acetic acid to give 0.65 g (100% yield) as a thick oil which solidified on standing.
Workup
- customto give 0.65 g (100% yield) as a thick oil which
Sources & evidence
- ORD record
- ord-00d8476672d546e589490e539c50c498
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08754095B2
Reaction notes
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