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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249893Generated: October 31, 2026

Sodium hydride → HCID 66873650, compound

https://huagongshe.com/reaction/249893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantHCID 44220648HCID 44220648—
ReactantMethyl 2-chlorobenzo[d]oxazole-4-carboxylateHCID 56924368—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 66873650HCID 6687365039%

Reaction Steps

To (S)-4-tert-butyloxycarbonyl-2-tert-butylpiperazine (640 mg, 2.6 0 mmol) in DME (10 mL) at room temperature, was added NaH (60% suspension in mineral oil, 115 mg, 3.50 mmol) and the mixture was stirred for 45 min. Methyl 2-chlorobenzoxazole-4-carboxylate (780 mg, 3.69 mmol) was added to the reaction mixture and the reaction was stirred at room temperature for 3d and at 55° C. for 24 h. The reaction mixture was quenched with CH3OH (10 mL), silica gel (15 mL) was added, and solvent removed under reduced pressure. The residue was purified by column chromatography (silica gel, 33% EtOAc in hexanes) to afford (S)-methyl 2-(4-tert-butyloxycarbonyl-2-tert-butyl-piperazin-1-yl)benzoxazole-4-carboxylate (0.42 g, 39%) as a yellow solid. 1H NMR and MS consistent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863271B2
Source datasetuspto-grants-2011_01
ORD IDord-0165dcb8eade4dde908b330b17ed6ce2
Source noteuspto-grants-2011_01