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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424982Generated: November 1, 2026

HCID 86648519, compound → Ethyl 2-[bis(tert-butoxycarbonyl)amino]-4-(1-hydroxypropyl)-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/1424982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86648519HCID 86648519—
ReactantHCID 178418443HCID 178418443—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDiethyl EtherHCID 3283—
ProductEthyl 2-[bis(tert-butoxycarbonyl)amino]-4-(1-hydroxypropyl)-1,3-thiazole-5-carboxylateHCID 6754897433%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Ethyl 2-[bis(tert-butoxycarbonyl)amino]-4-formyl-1,3-thiazole-5-carboxylate obtained in Example (62d) (915.5 mg, 2.29 mmol) was dissolved in diethyl ether (30 mL), followed by cooling to −78° C. Then, tetrabutylammonium bromide (890 mg, 2.76 mmol) and ethylmagnesium bromide (1 M solution in THF, 2.8 mL) were added, and the mixture was stirred for one hour. Diethyl ether was added to the reaction solution, and the organic layer was washed with brine and dried over anhydrous sodium sulfate. Following concentration under reduced pressure, the residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=91/9, 85/15) to obtain 327.2 mg of the title compound (33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927588B2
Source datasetuspto-grants-2015_01
ORD IDord-51469568ce6f4934873214bfd9a130c4
Source noteuspto-grants-2015_01