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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189393Generated: October 31, 2026

Nitrogen → HCID 67128714, compound

https://huagongshe.com/reaction/1189393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantSodium hydrideHCID 24758—
ReactantHCID 67128598HCID 67128598—
ReactantHCID 86664912HCID 86664912—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67128714HCID 67128714—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of [2-(3-acetyl-pyrazol-1-ylmethyl)-oxazol-4-yl]-carbamic acid tert-butyl ester (76 mg, 0.25 mmol) in THF (1.0 mL) was added to a suspension of NaH (27 mg, 0.61 mmol) in THF (0.5 mL) at 0° C. The resulting suspension was stirred at 0° C. for 5 min and at rt for 30 min. It was cooled to 0° C. and treated dropwise with a solution of the above prepared 2-cyclopropyl-5-phenyl-thiazole-4-carbonyl chloride in THF (1.0 mL). The resulting suspension was stirred for 30 min at 0° C. followed by 16 h at rt. Water was then added and the aq. layer was extracted several time with EA. The combined org. extracts were dried over Na2SO4, filtered, and the solvent was removed under reduced pressure. Purification of the residue by FC (6:4 hept-EA) gave the title compound as a yellow oil. TLC: rf (6:4 hept-EA)=0.20. LC-MS-conditions 02: tR=1.11 min, [M+H]+=534.30.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674111B2
Source datasetuspto-grants-2014_03
ORD IDord-6e4d6c96a3464d45bdd11720bde93437
Source noteuspto-grants-2014_03