Methylamine → HCID 68907656, compound
Reaction equation
[ClH:1].[F:2][C:3]1[CH:4]=[C:5]([C@@:9]([N:21]2[C:29]3[C:24](=[CH:25][CH:26]=[C:27]([O:30][CH3:31])[CH:28]=3)[CH:23]=[CH:22]2)(C2C=CC=CC=2)[C@H:10]([OH:14])[CH2:11][NH:12][CH3:13])[CH:6]=[CH:7][CH:8]=1.COC1C=C2C(C=CN2[C@@H](C2C=CC=C(F)C=2)[C@H](O)COS(C2C=CC(C)=CC=2)(=O)=O)=CC=1.CN>>[ClH:1].[F:2][C:3]1[CH:4]=[C:5]([C@H:9]([N:21]2[C:29]3[C:24](=[CH:25][CH:26]=[C:27]([O:30][CH3:31])[CH:28]=3)[CH:23]=[CH:22]2)[C@H:10]([OH:14])[CH2:11][NH:12][CH3:13])[CH:6]=[CH:7][CH:8]=1Participants
4
Procedure
In an analogous manner to EXAMPLE 5, (1S,2R)-1-(3-fluorophenyl)-1-(6-methoxy-1H-indol-1-yl)-3-(methylamino)-1-phenylpropan-2-ol hydrochloride was prepared from (2S,3S)-toluene-4-sulfonic acid 3-(6-methoxy-indol-1-yl)-2-hydroxy-3-(3-fluorophenyl)-propyl ester and methylamine as a white solid. MS (ES) m/z 329.2; HRMS: calcd for C19H21FN2O2+H+, 329.16598; found (ESI, [M+H]+), 329.1663.
Sources & evidence
- ORD record
- ord-831e036fd9fd4326b667776391c59db1
- Source dataset
- uspto-grants-2009_04
- Patent number
- US07517899B2
Reaction notes
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