Hydrogen Bromide → HCID 17967160, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:9]=[C:10]([CH2:14][NH:15][CH2:16][CH:17]3[CH2:26][CH2:25][C:24]4[C:19](=[C:20]([O:27]C)[CH:21]=[CH:22][CH:23]=4)[O:18]3)[CH:11]=[N:12][CH:13]=2)=[CH:4][CH:3]=1.[BrH:29]>>[BrH:29].[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:9]=[C:10]([CH2:14][NH:15][CH2:16][CH:17]3[CH2:26][CH2:25][C:24]4[C:19](=[C:20]([OH:27])[CH:21]=[CH:22][CH:23]=4)[O:18]3)[CH:11]=[N:12][CH:13]=2)=[CH:4][CH:3]=1Participants
3
Procedure
Analoguosly to example 2.1, (2R/S)-2-({[5-(4-fluorophenyl)-pyridin-3ylmethyl]-amino}-methyl)-8-methoxychroman is treated with hydrobromic acid to obtain (2R/S)-2-({[5-(4-fluorophenyl)-pyridin-3ylmethyl]-amino}-methyl)-chroman-8-ol hydrobromide.
Sources & evidence
- ORD record
- ord-ee2b9029a9ed4ff7a4163f5ae6ecb9f7
- Source dataset
- uspto-grants-2009_11
- Patent number
- US07618988B2
Reaction notes
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