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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025741Generated: November 1, 2026

Benzaldehyde → N-[2-({(3R)-1-[cis-2-(Benzylamino)cyclohexyl]pyrrolidin-3-yl]amino)-2-oxoethyl]-3-(trifluoromethyl)benzamide

https://huagongshe.com/reaction/1025741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN-(2-{[(3R)-1-(cis-2-aminocyclohexyl)pyrrolidin-3-yl]amino}-2-oxoethyl)-3-(trifluoromethyl)benzamideHCID 66787120—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductN-[2-({(3R)-1-[cis-2-(Benzylamino)cyclohexyl]pyrrolidin-3-yl]amino)-2-oxoethyl]-3-(trifluoromethyl)benzamideHCID 6678712769.6%

Reaction Steps

To a mixture of benzaldehyde (0.061 mL, 0.6 mmol) and N-(2-{[(3R)-1-(cis-2-aminocyclohexyl)pyrrolidin-3-yl]amino}-2-oxoethyl)-3-(trifluoromethyl)benzamide (0.278 g, 0.60 mmol) in CH2Cl2 (10 mL) was added NaB(OAc)3H (0.128 g, 0.60 mmol). After being stirred overnight at room temperature under N2, the reaction mixture was diluted with EtOAc and washed with saturated Na2CO3. The aqueous layer was extracted with EtOAc (3×). The combined organic layers were dried (MgSO4), concentrated and flash chromatographed (EtOAc to EtOAc:MeOH:Et3N=9:1:0.5) to give 0.21 g of the title compound. MS (EI) calcd: (M+H)+=503.3; found: 503.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729063B2
Source datasetuspto-grants-2014_05
ORD IDord-70c09694373b47e28e32572d903e2fea
Source noteuspto-grants-2014_05