Hydrochloric Acid → 5-(4-Methyl-thiazol-2-yl)-2,3-dihydro-1H-isoindole
Reaction equation
C(OC([N:8]1[CH2:16][C:15]2[C:10](=[CH:11][CH:12]=[C:13]([C:17]3[S:18][CH:19]=[C:20]([CH3:22])[N:21]=3)[CH:14]=2)[CH2:9]1)=O)(C)(C)C.Cl>>[CH3:22][C:20]1[N:21]=[C:17]([C:13]2[CH:14]=[C:15]3[C:10](=[CH:11][CH:12]=2)[CH2:9][NH:8][CH2:16]3)[S:18][CH:19]=1Participants
3
Procedure
Prepared in analogy to Example A3(e) from 5-(4-Methyl-thiazol-2-yl)-1,3-dihydro-isoindole-2-carboxylic acid tert-butyl ester and using trifluoacetic acid instead of hydrochloride acid. Brown solid. MS (m/e): 217.1 ([M+H]+, 100%)
Sources & evidence
- ORD record
- ord-4faf4fcb9369433fb726abc2d9924fb5
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07557114B2
Reaction notes
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