Diisopropylethylamine → HCID 67974886, compound
Reaction equation
Cl.[Cl:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[NH:8][CH:7]=[C:6]2[CH2:12][CH2:13][NH2:14].[F:15][C:16]1[CH:24]=[C:23]([CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[C:28]([F:32])[CH:27]=2)[CH:22]=[CH:21][C:17]=1[C:18](O)=[O:19].CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C(N(CC)C(C)C)(C)C>CN(C=O)C>[Cl:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[NH:8][CH:7]=[C:6]2[CH2:12][CH2:13][NH:14][C:18](=[O:19])[C:17]1[CH:21]=[CH:22][C:23]([CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[C:28]([F:32])[CH:27]=2)=[CH:24][C:16]=1[F:15]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
N-(2-(5-Chloro-1H-indol-3-yl)ethyl)-2-fluoro-4-(3-fluorobenzyl)benzamide was prepared according to Method A starting from 2-(5-chloro-1H-indol-3-yl)ethanamine hydrochloride (0.075 g; 0.318 mmol), 2-fluoro-4-(3-fluorobenzyl)benzoic acid (0.087 g; 349 mmol), HATU (0.121 g: 0.318 mmol) and N,N-diisopropylethylamine (0.139 mL; 0.795 mmol) in DMF (5 mL). Flash chromatography on silica gel (eluent 0 to 10% of ethyl acetate in dichloromethane) followed by recrystallization from a mixture of dichloromethane/heptane, furnished 0.098 g (73%) of the title compound as a white solid.
Workup
- customN-(2-(5-Chloro-1H-indol-3-yl)ethyl)-2-fluoro-4-(3-fluorobenzyl)benzamide was prepared
- customFlash chromatography on silica gel (eluent 0 to 10% of ethyl acetate in dichloromethane) followed by recrystallization from a mixture of dichloromethane/heptane
Sources & evidence
- ORD record
- ord-ff8dd6bd58684c77a6b6dff604c5193e
- Source dataset
- uspto-grants-2016_02
- Patent number
- US09266832B2
Reaction notes
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