Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713514Generated: November 3, 2026

2-Chlorobenzoxazole → HCID 23121962, compound

https://huagongshe.com/reaction/1713514

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzoxazoleHCID 11986—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,1-Diphenyltetrahydro-1H-oxazolo[3,4-a]pyrazin-3(5H)-oneHCID 23121881—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23121962HCID 2312196262%

Reaction Steps

To a solution of hexahydro-1,1-diphenyl-3H-oxazolo[3,4-a]pyrazin-3-one (60 mg, 0.2 mmol) in tetrahydrofuran (2 mL) were sequentially added diisopropylethylamine (0.3 mL) and 2-chlorobenzoxazole (45 mg, 0.29 mmol), and the mixture was stirred at room temperature for 3 hours. The reaction solution was concentrated under reduced pressure. Then, the residue was purified with silica gel column chromatography (hexane:ethyl acetate=3:1) and recrystallized from diisopropyl ether to obtain the title compound (51 mg, yield 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795267B2
Source datasetuspto-grants-2010_09
ORD IDord-1cd5431f046b41caa83c8a74358ce6ec
Source noteuspto-grants-2010_09