Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415334Generated: October 29, 2026

Pyridine → HCID 66621249, compound

https://huagongshe.com/reaction/415334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 66620870HCID 66620870—
SolventTolueneHCID 1140—
ProductHCID 66621249HCID 6662124926%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of methyl 3-(4-(2-((benzyloxycarbonyl)(methyl)amino)ethyl)benzamido)-2-hydroxybenzoate (800 mg, 1.73 mmol) in anhydrous toluene (10 mL) was added anhydrous pyridine (0.76 mL, 9.5 mmol), then thionyl chloride (0.7 ml, 9.5 mmol) was added. The mixture was heated to 110° C. for 2 h. The mixture was cooled to room temperature and poured into ice water (100 mL) carefully with vigorous stirring, then extracted with ethyl acetate (50 mL×3). The organic phase was washed with saturated sodium bicarbonate solution and brine, dried over anhydrous sodium sulfate, and concentrated to give crude product. The crude product was purified by prep-HPLC to give methyl 2-(4-(2-((benzyloxycarbonyl)(methyl)amino)ethyl)phenyl)benzo[d]oxazole-7-carboxylate 200 mg, yield 22%). LC-MS (ESI) m/z: 445 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088760B2
Source datasetuspto-grants-2012_01
ORD IDord-69c5e0feeb4940d1ad9ea602cde281c5
Source noteuspto-grants-2012_01