1-Hydroxy-1-cyclopropanecarboxylic acid → HCID 178523660, compound
Reaction equation
Cl.Cl.[O:3]1[C:8]2=[CH:9][CH:10]=[CH:11][C:7]2=[CH:6][C:5]([CH:12]2[CH2:17][CH2:16][CH2:15][CH2:14][N:13]2[CH2:18][CH2:19][C@H:20]2[CH2:25][CH2:24][C@H:23]([NH2:26])[CH2:22][CH2:21]2)=[CH:4]1.[OH:27][C:28]1([C:31](O)=[O:32])[CH2:30][CH2:29]1>>[O:3]1[C:8]2=[CH:9][CH:10]=[CH:11][C:7]2=[CH:6][C:5]([CH:12]2[CH2:17][CH2:16][CH2:15][CH2:14][N:13]2[CH2:18][CH2:19][C@H:20]2[CH2:21][CH2:22][C@H:23]([NH:26][C:31]([C:28]3([OH:27])[CH2:30][CH2:29]3)=[O:32])[CH2:24][CH2:25]2)=[CH:4]1Participants
3
Procedure
The title compound, white solid (67 mg, 65%), MS (ISP) m/z=411.3 [(M+H)+], mp 200° C., was prepared in accordance with the general method of example 1 from trans-4-[2-(4-benzofuran-3-yl-piperidin-1-yl)-ethyl]-cyclohexylamine dihydrochloride (intermediate A) (100 mg, 0.25 mmol) and 1-hydroxy-cyclopropanecarboxylic acid.
Sources & evidence
- ORD record
- ord-676b59f2efbd42369d1b2fe1c3f41ec4
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08921397B2
Reaction notes
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