Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132215Generated: October 31, 2026

Toluene → HCID 59731886, compound

https://huagongshe.com/reaction/132215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 59731971HCID 59731971—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 59731886HCID 5973188644%

Reaction Conditions

Temperature60 °C

Reaction Steps

4-Amino-1-N-Boc-piperidine (290 mg, 1.4 mmol) was added to a solution of ethyl 3-formylpyridin-2-ylcarbamate (240 mg, 1.2 mmol) in methanol (10 mL). Mixture was warmed to 60° C. and held for 1.5 hours. Mixture was cooled to room temperature. Sodium borohydride (62 mg, 1.6 mmol) was added to the mixture. Reaction stirred at room temperature for 30 minutes. Toluene (20 mL) was added to the mixture followed by acetic acid (1.0 mL). Mixture was warmed to 110° C. Methanol was driven from the reaction mixture and collected in a Dean-Stark trap. Mixture was held at 110° C. for 5 hours. Mixture was cooled to room temperature and held for 16 hours. Reaction was quenched with aqueous sodium bicarbonate. Mixture was extracted with ethyl acetate (2×30 mL). Combined organics were washed successively with water (30 mL) and brine (20 mL). Organic layer was dried (magnesium sulfate), filtered and concentrated in vacuo. Silica gel chromatography afforded the title compound as white solid in 44% yield. MS m/e (M−H)−=311.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384930B2
Source datasetuspto-grants-2008_06
ORD IDord-787df35f5ada419fb3589ff9daef2b0b
Source noteuspto-grants-2008_06