Hydrochloric Acid → 5-Chloro-6-morpholin-4-yl-2,3-dihydro-1H-isoindole hydrochloride
Reaction equation
C(OC([N:8]1[CH2:16][C:15]2[C:10](=[CH:11][C:12]([N:18]3[CH2:23][CH2:22][O:21][CH2:20][CH2:19]3)=[C:13]([Cl:17])[CH:14]=2)[CH2:9]1)=O)(C)(C)C.Cl>>[ClH:17].[Cl:17][C:13]1[CH:14]=[C:15]2[C:10](=[CH:11][C:12]=1[N:18]1[CH2:19][CH2:20][O:21][CH2:22][CH2:23]1)[CH2:9][NH:8][CH2:16]2Participants
3
Procedure
Prepared in analogy to Example A3(e) from 5-chloro-6-morpholin-4-yl-1,3-dihydro-isoindole-2-carboxylic acid tert-butyl ester and hydrochloric acid. Off-white solid. MS (m/e): 241.4 ({37Cl}M+H+, 52%), 239.3 ({35Cl}M+H+, 100%).
Sources & evidence
- ORD record
- ord-4d7c1115dfa54ef0ad90d522556da6f7
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07557114B2
Reaction notes
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