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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449529Generated: October 31, 2026

Triphenylphosphine → HCID 19978109, compound

https://huagongshe.com/reaction/1449529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantEthyl GlycolateHCID 12184—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 178522178HCID 178522178—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19978109HCID 19978109—

Reaction Conditions

Temperature-78 °C

Reaction Steps

In 40 ml of tetrahydrofuran was dissolved 916 mg of triphenylphosphin. To the solution was added 550 μl of azodicarboxylic acid diethylester under cooling with ice, followed by cooling to -78° C. To the reaction mixture was added 1.0 g of N-(3,5-dichlorophenyl)-6,7-dihydro-3-hydroxy-5H-thiazolo[3,2-a]pyrimidine-2-carboxamide obtained in Example 111 and 400 μl of hydroxyacetic acid ethylester, followed by raising the reaction temperature to room temperature by the degree. After stirring at room temperature for 1 hour, the solvent was removed under reduced pressure. The residue was purified by silica gel column chromatography (silica gel:50 g) using chloroform and metanol (20:1 by volume) as an eluent to obtain 1.00 g of the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05599813
Source datasetuspto-grants-1997_02
ORD IDord-c14721513f19440b92ab830b933410af
Source noteuspto-grants-1997_02