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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249894Generated: October 31, 2026

Potassium Carbonate → HCID 66873354, compound

https://huagongshe.com/reaction/249894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 12197172HCID 12197172—
ReactantMethyl 2-chlorobenzo[d]oxazole-4-carboxylateHCID 56924368—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 66873354HCID 6687335460%

Reaction Conditions

Temperature35 °C

Reaction Steps

A mixture of methyl 2-chlorobenzoxazole-4-carboxylate (970 mg, 4.58 mmol) and (3S,5S)-1-benzyl-3,5-dimethylpiperazin-2-one (1.00 g, 4.58 mmol) in DMF (20 mL), was stirred in a 35° C. oil bath. After 16 h, the reaction mixture was heated to 55° C. After 3 h, potassium carbonate (630 mg, 4.58 mmol) was added. The reaction mixture was stirred for 2 h at 55° C. and then at ambient temperature for 17 h. The reaction mixture was diluted with H2O (50 mL) and extracted with EtOAc (2×50 mL). The combined organic layers were washed with 0.5 N HCl (25 mL), H2O (25 mL), brine (25 mL), dried (Na2SO4), and concentrated under reduced pressure. Purification by chromatography (silica gel, 10 to 80% EtOAc in hexanes) gave methyl 2-((2S,6S)-4-benzyl-2,6-dimethyl-3-oxopiperazine-1-yl)benzoxazole-4-carboxylate (1.08 g, 60%). 1H NMR consistent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863271B2
Source datasetuspto-grants-2011_01
ORD IDord-cbc49de61db340d68c21479643df5e82
Source noteuspto-grants-2011_01