Pyrrolidine → Methyl 2'-fluoro-5'-(methyloxy)-2-(1-pyrrolidinylmethyl)-1,1'-biphenyl-4-carboxylate
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][C:3]=1[C:10]1[CH:15]=[CH:14][C:13]([C:16]([O:18][CH3:19])=[O:17])=[CH:12][C:11]=1[CH2:20][N:21]1C[CH2:25][CH2:24][CH2:23][CH2:22]1.N1CCCC1>>[F:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][C:3]=1[C:10]1[CH:15]=[CH:14][C:13]([C:16]([O:18][CH3:19])=[O:17])=[CH:12][C:11]=1[CH2:20][N:21]1[CH2:22][CH2:23][CH2:24][CH2:25]1Participants
3
Procedure
Compound 66.65A was synthesized using a procedure analogous to that used for 66.64A using pyrrolidine in place of piperidine. MS ESI (pos.) m/e: 344 (M+H)+.
Sources & evidence
- ORD record
- ord-ac5e085b30a9405484a5cdd988bc70ea
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08030354B2
Reaction notes
Loading…