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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842781Generated: November 1, 2026

Acetic Acid → (2-(1-(2-Cyano-4-trifluoromethylphenyl)piperidin-4-ylamino)-ethyl)carbamic acid tert-butyl ester

https://huagongshe.com/reaction/842781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1,1-DichloroethaneHCID 6365—
ReactantN-BOC-ethylenediamineHCID 187201—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantN-(2-Cyano-4-trifluoromethylphenyl)-4-piperidoneHCID 22615393—
SolventMethanolHCID 887—
Product(2-(1-(2-Cyano-4-trifluoromethylphenyl)piperidin-4-ylamino)-ethyl)carbamic acid tert-butyl esterHCID 18727097—

Reaction Steps

A solution of 25 (535 mg, 1.99 mmol), 1 (335 mg, 2.09 mmol), and acetic acid (629 mg, 10.48 mmol) in methanol(2 mL)/dichloroethane(1 mL) was treated with sodium cyanoborohydride (130 mg, 2.06 mmol) at room temperature. The resulting mixture was stirred at room temperature overnight. The solvent was removed in vacuo and the residue dissolved in dichloromethane and sodium carbonate solution. The aqueous layer was extracted with two additional portions of dichloromethane and the combined organic extracts were washed with brine, dried over Na2SO4, and concentrated under reduced pressure. PCTLC (SiO2, 4 mm, 10% EtOH-90% CHCl3) afforded the title compound (26).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376503B1
Source datasetuspto-grants-2002_04
ORD IDord-d87d1e5e969244feadcc07b3064c15af
Source noteuspto-grants-2002_04