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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406245Generated: October 31, 2026

tert-Butyl 4-oxopiperidine-1-carboxylate → HCID 67980795, compound

https://huagongshe.com/reaction/2406245

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 88540108HCID 88540108—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 67980795HCID 67980795204.5%

Reaction Steps

To a vial containing 4-((R)-3-morpholin-4-yl-1-phenyl-sulfanylmethyl-propylamino)-N-(5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazin-3-yl)-3-trifluoromethanesulfonyl-benzenesulfonamide (50 mg, 0.074 mmol) and 4-oxo-piperidine-1-carboxylic acid tert-butyl ester (14.74 mg, 0.074 mmol) was added methanol (2 mL) under nitrogen. The reaction mixture was stirred in an ice bath for 10 minutes, and then acetic acid (0.424 μL, 7.40 μmol) was added. The reaction mixture was stirred for another 30 minutes. Sodium cyanoborohydride (41.85 mg, 0.666 mmol) was then added, and the reaction was stirred at ambient temperature for 72 hours. The reaction mixture was concentrated, filtered and purified via flash chromatography on silica gel (10-50% 7N NH3 in methanol in CH2Cl2) to afford 4-{3-[4-((R)-3-Morpholin-4-yl-1-phenylsulfanylmethyl-propylamino)-3-trifluoromethanesulfonyl-benzenesulfonylamino]-5,6-dihydro-8H-[1,2,4]triazolo[4,3-a]pyrazin-7-yl}-piperidine-1-carboxylic acid tert-butyl ester (65 mg, 100% yield). MS [m/z; (M+1)+]: 859.7

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809352B2
Source datasetuspto-grants-2014_08
ORD IDord-8769df45335c403e89e81197b567902b
Source noteuspto-grants-2014_08