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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716902Generated: October 31, 2026

tert-Butyl 4-oxopiperidine-1-carboxylate → HCID 58997385, compound

https://huagongshe.com/reaction/1716902

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 58997363HCID 58997363—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 58997385HCID 5899738590.4%

Reaction Steps

Place N-(6-aminopyridin-2-yl)-4-fluorobenzamide (Preparation 37) (2 g, 8.3 mmol) and 1-boc-4-piperidone (15.0 g, 83 mmol) in 1,2-dichloroethane (20 mL). Stir for 1 hr. then add sodium triacetoxyborohydride (4.38 g, 20.8 mmol). After stirring for 36 hr., quench with 1 N NaOH and dilute with CH2Cl2. Separate and extract the aqueous layer twice with CH2Cl2, combine organics, dry over MgSO4, and concentrate. Take up the residue in CH2Cl2, and place on two 10 g SCX columns. Wash the columns successively with CH2Cl2 and then with methanol. Elute the product with 2M NH3 in methanol. Concentrate and chromatograph on silica gel, eluting with a gradient of 0-10% (2M NH3 in methanol) in CH2Cl2) to give the title intermediate 3.11 g (90%): mass spectrum (ion spray): m/z 415.4 (M+1); mp 82.7° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803813B2
Source datasetuspto-grants-2010_09
ORD IDord-61ff6342f2d14d78ad9576eb600ce317
Source noteuspto-grants-2010_09