Hydrochloric Acid → 5-Chloro-6-piperidin-1-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][CH2:21][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[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]1)[CH2:9][NH:8][CH2:16]2Participants
3
Procedure
Prepared in analogy to Example A3(e) from 5-chloro-6-piperidin-1-yl-1,3-dihydro-isoindole-2-carboxylic acid tert-butyl ester and hydrochloric acid. Brown solid. MS (m/e): 239.2 ({37Cl}M+H+, 35%), 237.1 ({35Cl}M+H+, 100%).
Sources & evidence
- ORD record
- ord-da7922ba98d74a298567aed8dd93e9b6
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07557114B2
Reaction notes
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