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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245834Generated: November 2, 2026

Hydrochloric Acid → HCID 68680811, compound

https://huagongshe.com/reaction/2245834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantBiphenyl-2-ylcarbamic Acid Piperidin-4-yl EsterHCID 10851461—
ReactantHCID 68680479HCID 68680479—
SolventAcetonitrileHCID 6342—
ProductHCID 68680811HCID 6868081152%

Reaction Steps

To crude 1-[3-(tert-butyldimethylsilanyloxy)propyl]-3-(3,3-dimethoxypropyl)imidazolidin-2-one (11.4 g, 32 mmol; prepared as described in Preparation 2) was added to a 1:1 mixture of 1N aqueous HCl (32 mL, 32 mmol, 1.0 eq) in ACN (32 mL). The reaction was allowed to stir at room temperature for 2 hours. To the reaction mixture was added biphenyl-2-ylcarbamic acid piperidin-4-yl ester (9.4 g, 32 mmol; prepared as described in Preparation 3) and was allowed to stir for 30 minutes, followed by the addition of NaBH(OAc)3 (20.3 g, 96 mmol). The reaction mixture was allowed to stir overnight. After overnight, the solution was concentrated in vacuo. The crude mixture was taken up in DCM (400 mL) and washed with 1N NaOH (200 mL), water (200 mL) and brine (200 mL). The organic phase was dried over MgSO4, filtered and concentrated then purified via silica gel chromatography (10% MeOH in DCM with 1% NH3(aq)) to afford the title compound (7.98 g, 16.6 mmol) in 52% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683173B2
Source datasetuspto-grants-2010_03
ORD IDord-e8ec1a0755e648c2a5c656d1e2b0fd18
Source noteuspto-grants-2010_03