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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433754Generated: October 30, 2026

Pyridine → HCID 68620162, compound

https://huagongshe.com/reaction/1433754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 68618190HCID 68618190—
SolventDichloromethaneHCID 6344—
ProductHCID 68620162HCID 6862016251%

Reaction Steps

To a solution of (2R)-(4-amino-phenyl)-tert-butoxycarbonylamino-acetic acid (100 mg, 0.376 mmol) in dichloromethane (2 mL) was added pyridine (36 μL, 0.45 mmol) and acetic anhydride (42 μL, 0.44 mmol) and the mixture stirred at ambient temperature for 2 hours. The reaction mixture was diluted with dichloromethane, washed with 1M aqueous citric acid solution, brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by chromatography over silica gel gradient eluted from 0 to 10% v/v methanol in dichloromethane to afford (2R)-(4-acetylamino-phenyl)-tert-butoxycarbonylamino-acetic acid as a yellow solid (59 mg, 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612212B2
Source datasetuspto-grants-2009_11
ORD IDord-cee464faa3004ad882a94cc623667895
Source noteuspto-grants-2009_11