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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604488Generated: October 30, 2026

Ethyl Acetate → [5-(3-Methyl-[1,2,4]oxadiazol-5-yl)-4-phenyl-thiazol-2-yl]-carbamic Acid tert-butyl ester

https://huagongshe.com/reaction/604488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
ReactantHCID 50742682HCID 50742682—
ReactantHCID 178465666HCID 178465666—
SolventTetrahydrofuranHCID 8028—
Product[5-(3-Methyl-[1,2,4]oxadiazol-5-yl)-4-phenyl-thiazol-2-yl]-carbamic Acid tert-butyl esterHCID 5770959936%

Reaction Steps

2-Tert-butoxycarbonylamino-4-phenyl-thiazole-5-carboxylic acid ethyl ester (1.9 g 5.6 mmol) was dissolved in dry THF (60 mL). Sodium hydride (60% in oil) and N-hydroxy-acetamidine (0.83 g, 11.2 mmol) dissolved in THF (30 mL) was added. The reaction mixture was heated to reflux over night. The reaction mixture was cooled and ethyl acetate (75 mL) glacial acetic acid (0.43 g) were added. The organic mixture was washed with brine (75 mL). The aqueous phase was extracted with ethylacetate The combined organic phases was washed with brine (50 mL) dried with MgSO4 and solvents were removed in vacuo to give a solid. Yield: 36%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910613B2
Source datasetuspto-grants-2011_03
ORD IDord-1fc7453889f240fc94996d1a9dc9328a
Source noteuspto-grants-2011_03