Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500523Generated: November 1, 2026

Sodium Hydroxide → HCID 86700513, compound

https://huagongshe.com/reaction/1500523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantBenzyl 4-oxopiperidine-1-carboxylateHCID 643496—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(S)-1-Boc-3-methylpiperazineHCID 7023035—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 86700513HCID 8670051334.1%

Reaction Steps

To a solution of (S)-3-methyl-piperazine-1-carboxylic acid tert-butyl ester (1.0 g, mmol) and N-benzyloxycarbonyl-4-piperidone (1.2 g, 5 mmol) in methanol (8 mL) was added acetic acid (0.28 mL) and the solution was stirred at RT for 1 h. Sodium cyanoborohydride (310 mg, 5 mmol) was added and the reaction mixture was stirred at 45° C. overnight and then 1 N NaOH (5 mL) was added. The aqueous phase was extracted with EtOAc (3×15 mL). The combined organic extracts were washed with brine, dried over MgSO4, filtered, concentrated under vacuum, and purified by silica gel chromatography (0-5% MeOH/DCM). Pure fractions were combined and concentrated under vacuum to provide the title intermediate (0.71 g, 30% yield) as a clear oil. (m/z): [M+H]+ calcd for C23H35N3O4 418.26 found 418.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206159B2
Source datasetuspto-grants-2015_12
ORD IDord-660354e46fbe40568b1b4e003a0132ac
Source noteuspto-grants-2015_12