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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098376Generated: October 31, 2026

Pyridine → HCID 57920212, compound

https://huagongshe.com/reaction/2098376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantOxalyl chlorideHCID 65578—
Reactant3-(1,3-Oxazol-5-yl)anilineHCID 2739289—
Reactant1-[(Tert-butoxy)carbonyl]-4-methylpiperidine-4-carboxylic acidHCID 23282848—
ReactantTert-butyl 4-methyl-4-(3-(oxazol-5-yl)phenylcarbamoyl)piperidine-1-carboxylateHCID 67036759—
CatalystDimethylformamideHCID 6228—
Solvent1,2-DichloroethaneHCID 11—
SolventEthyl AcetateHCID 8857—
ProductHCID 57920212HCID 57920212—

Reaction Steps

Preparation of tert-butyl 4-methyl-4-(3-(oxazol-5-yl)phenylcarbamoyl)piperidine-1-carboxylate. To a solution of 1-(tert-butoxycarbonyl)-4-methylpiperidine-4-carboxylic acid (61.3 mg, 0.252 mmol) and pyridine (79.7 mg, 0.08 mL, 1.01 mmol) in 1,2-dichloroethane (2 mL) at 0° C. was added DMF (1-2 drops) followed by oxalyl chloride (31.9 mg, 0.022 mL, 0.252 mmol). The reaction was stirred for 0.5 hour, and 3-(oxazol-5-yl)aniline (40.4 mg, 0.252 mmol) was added. The reaction was allowed to stir for another 1.5 hours. The mixture was diluted with ethyl acetate (10 mL), and the organics were washed with 0.1 N HCl (2×10 mL), brine (4 mL), dried over MgSO4, filtered, and concentrated to give the title compound, which was used in the next step without further purification. MS (ES+) [M+H]+386.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450332B2
Source datasetuspto-grants-2013_05
ORD IDord-dfa20defd3cc4051b90c1b015fe29612
Source noteuspto-grants-2013_05