Trifluoroacetic acid → 5-Ethyl-6-(tetrahydro-pyran-4-yl)-2,3-Dihydro-1H-isoindole trifluoro-acetate
Reaction equation
C(OC([N:8]1[CH2:16][C:15]2[C:10](=[CH:11][C:12]([CH:19]3[CH2:24][CH2:23][O:22][CH2:21][CH2:20]3)=[C:13]([CH2:17][CH3:18])[CH:14]=2)[CH2:9]1)=O)(C)(C)C.[F:25][C:26]([F:31])([F:30])[C:27]([OH:29])=[O:28]>>[F:25][C:26]([F:31])([F:30])[C:27]([OH:29])=[O:28].[CH2:17]([C:13]1[CH:14]=[C:15]2[C:10](=[CH:11][C:12]=1[CH:19]1[CH2:24][CH2:23][O:22][CH2:21][CH2:20]1)[CH2:9][NH:8][CH2:16]2)[CH3:18]Participants
3
Procedure
Prepared in analogy to Example A2(c) from 5-ethyl-6-(tetrahydro-pyran-4-yl)-1,3-dihydro-isoindole-2-carboxylic acid tert-butyl ester and trifluoroacetic acid. Yellow oil. MS (m/e): 232.1 ([M+H]+, 100%).
Sources & evidence
- ORD record
- ord-aa46427ebc7a495b83dee6142df59f0c
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07557114B2
Reaction notes
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