Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099351Generated: November 1, 2026

Sodium triacetoxyborohydride → HCID 68828337, compound

https://huagongshe.com/reaction/2099351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl 2-oxopiperidine-1-carboxylateHCID 7577838—
ReactantHCID 68829063HCID 68829063—
SolventDichloromethaneHCID 6344—
ProductHCID 68828337HCID 6882833765.6%

Reaction Steps

0.41 g of N-[8-(4-chloro-D-phenylalanyl)-8-azabicyclo[3.2.1]oct-3-yl]-N-cyclohexyl-N′,N′-diethylurea is dissolved in 4 ml of dichloromethane under N2 in the presence of 0.17 g of N-BOC-piperidone and of 0.23 g of sodium triacetoxyborohydride, and the mixture is stirred at ambient temperature for 16 h. After evaporation and hydrolysis, extraction is carried out with ethyl acetate until the aqueous phase is completely depleted. The organic phase is washed with H2O and then with a saturated aqueous sodium chloride solution. Drying over MgSO4 and concentration to dryness are carried out. The crude is chromatographed on silica gel, elution being carried out with a 98/2 mixture of dichloromethane and methanol. 0.37 g of tert-butyl 4-{[(1R)-1-(4-chlorobenzyl)-2-(3-{cyclohexyl[(diethylamino)carbonyl]amino}-8-azabicyclo-[3.2.1]oct-8-yl)-2-oxoethyl]amino}piperidine-1-carboxylate is then obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569582B2
Source datasetuspto-grants-2009_08
ORD IDord-0b5e6f590b2b48d39c628b6a42fe775f
Source noteuspto-grants-2009_08