Potassium trifluoro[(pyrrolidin-1-yl)methyl]borate → 1-[4-(7-Fluoro-2,3-dihydro-benzo[1,4]dioxin-2-yl)-benzyl]-pyrrolidine
Reaction equation
[B-](F)(F)(F)CN1CCCC1.[K+].[F:12][C:13]1[CH:14]=[CH:15][C:16]2[O:21][CH2:20][CH:19]([C:22]3[CH:34]=[CH:33][C:25]([CH2:26][N:27]4[CH2:32][CH2:31]O[CH2:29][CH2:28]4)=[CH:24][CH:23]=3)[O:18][C:17]=2[CH:35]=1>>[F:12][C:13]1[CH:14]=[CH:15][C:16]2[O:21][CH2:20][CH:19]([C:22]3[CH:23]=[CH:24][C:25]([CH2:26][N:27]4[CH2:32][CH2:31][CH2:29][CH2:28]4)=[CH:33][CH:34]=3)[O:18][C:17]=2[CH:35]=1Participants
3
Procedure
The title compound is prepared from G-4 and Potassium 1-trifluoroboratomethylpyrrolidine according to the procedure described for the synthesis of compound 202. 203: LC/MS Method 10; Rt=1.07 min.; [M+H]+=354.4.
Sources & evidence
- ORD record
- ord-4ea7a01a7dc34a4e91e7b4bf66c76cbb
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09133146B2
Reaction notes
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