Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222410Generated: October 25, 2026

Acetic Acid → tert-Butyl {2-[(4-{1-[(1,5-dimethyl-1H-pyrazol-4-yl)methyl]piperidin-4-yl}benzoyl)amino]phenyl}carbamate

https://huagongshe.com/reaction/222410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium BicarbonateHCID 516892—
Reactant1,5-dimethyl-1H-pyrazole-4-carbaldehydeHCID 579643—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantTert-butyl 2-[(4-piperidin-4-ylbenzoyl)amino]phenylcarbamateHCID 59830875—
SolventDichloromethaneHCID 6344—
Producttert-Butyl {2-[(4-{1-[(1,5-dimethyl-1H-pyrazol-4-yl)methyl]piperidin-4-yl}benzoyl)amino]phenyl}carbamateHCID 5983088084%

Reaction Steps

1,5-Dimethyl-1H-pyrazole-4-carbaldehyde (114 mg, 0.92 mmol) was added to a solution of tert-butyl 2-[(4-piperidin-4-ylbenzoyl)amino]phenylcarbamate (289 mg, 0.73 mmol) in dichloromethane (6 ml) followed by acetic acid (50 μl, 0.87 mmol). The reaction mixture was allowed to stir under nitrogen for 2.5 hours. Sodium triacetoxyborohydride (233 mg, 1.10 mmol) was added and the reaction mixture allowed to stir, at ambient temperature, for 18 hours (overnight). Saturated aqueous sodium bicarbonate solution (10 ml) was then added to the reaction and allowed to stir for 15 minutes. The organic phase was separated and the aqueous phase re-extracted with dichloromethane (10 ml). The combined organics were washed with water, dried over magnesium sulphate and evaporated to dryness to afford the product as a colourless gum (308 mg, 84%), which was used without further purification; Mass Spectrum: M+H+504.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207202B2
Source datasetuspto-grants-2012_06
ORD IDord-cdca534bab4c44b887943abca852c687
Source noteuspto-grants-2012_06