Sodium triacetoxyborohydride → N-(2-Oxo-2-{[(3R)-1-(4-phenoxycyclohexyl)pyrrolidin-3-yl]amino}ethyl)-3-(trifluoromethyl)benzamide

HRID 1016020Notes

Reaction equation

HRID 1016020 reaction equation
[O:1]([CH:8]1[CH2:13][CH2:12][C:11](=O)[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[O:15]=[C:16]([NH:31][CH2:32][C:33](=O)[NH:34][C@@H:35]1[CH2:39]CNC1)[CH2:17][NH:18][C:19](=[O:30])[C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([C:26]([F:29])([F:28])[F:27])[CH:21]=1.[BH-](OC(C)=O)(OC(C)=O)OC(C)=O.[Na+]>CC(O)=O.C(Cl)Cl.CCOC(C)=O>[O:15]=[C:16]([NH:31][C@@H:32]1[CH2:39][CH2:35][N:34]([CH:11]2[CH2:12][CH2:13][CH:8]([O:1][C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)[CH2:9][CH2:10]2)[CH2:33]1)[CH2:17][NH:18][C:19](=[O:30])[C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([C:26]([F:29])([F:28])[F:27])[CH:21]=1

Participants

6

Reactant 3

HCID 5049666Sodium triacetoxyborohydrideHCID 224671324-PhenoxycyclohexanoneHCID 66787189N-[2-oxo-2-({2-oxo-2-[(3R)-pyrrolidin-3-ylamino]ethyl}amino)ethyl]-3-(trifluoromethyl)benzamide

Product 1

HCID 59556060N-(2-Oxo-2-{[(3R)-1-(4-phenoxycyclohexyl)pyrrolidin-3-yl]amino}ethyl)-3-(trifluoromethyl)benzamide

Reagents, catalysts & solvents 2

HCID 8857Ethyl AcetateSolventHCID 21922555Acetic acid methylene chlorideSolvent

Procedure

To a mixture of 4-phenoxycyclohexanone (0.091 g, 0.475 mmol) and N-[2-oxo-2-({2-oxo-2-[(3R)-pyrrolidin-3-ylamino]ethyl}amino)ethyl]-3-(trifluoromethyl)benzamide in 2% AcOH/CH2Cl2 (10 mL) was added NaB(OAc)3H (0.134 g, 0.634 mmol). After being stirred overnight at room temperature under N2, the reaction mixture was diluted with EtOAc and washed with saturated Na2CO3. The aqueous was extracted with EtOAc (3×). The combined organic layers were dried (MgSO4), concentrated and flash chromatographed (EtOAc to EtOAc:MeOH:Et3N=9:1:0.1) to give 0.12 g of the title compound. MS (EI) calcd: (M+H)+=490.2; found 490.0.

Workup

  1. washwashed with saturated Na2CO3
  2. extractionThe aqueous was extracted with EtOAc (3×)
  3. dry with materialThe combined organic layers were dried (MgSO4)
  4. concentrationconcentrated
  5. customflash chromatographed (EtOAc to EtOAc:MeOH:Et3N=9:1:0.1)

Sources & evidence

ORD record
ord-d740d57bcbe74b90a9eb7a08b98fce24
Source dataset
uspto-grants-2011_07
Patent number
US07985730B2

Reaction notes

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