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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581232Generated: October 30, 2026

Water → HCID 15435120, compound

https://huagongshe.com/reaction/581232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDabcoHCID 9237—
ReactantO,O-diethyl phosphorochloridothioateHCID 17305—
ReactantHCID 88204179HCID 88204179—
SolventDimethylacetamideHCID 31374—
ProductHCID 15435120HCID 15435120—

Reaction Conditions

Temperature2 °C

Reaction Steps

To a stirred suspension of 30 g (Z)-(RS)-(2-aminothiazol-4-yl)-[(tetrahydropyran-2-yloxyimino)]-acetic acid (80.5 mmol) and 90 mg 1,4-diazabicyclo[2.2.2]octane (DABCO) (0.80 mmol) in 300 ml dimethylacetamide was added under argon over 45 min 17 ml diethyl chlorothiophosphate (104.9 mmol). Stirring was continued at 0° C. for 1 h. The reaction was followed by HPLC. To the slightly turbid reaction mixture was added dropwise over 50 min 450 ml water. The precipitated product was filtered, washed with water and dissolved in dichloromethane. The aqueous layer was back-extracted with dichloromethane. The combined organic layers were dried over sodium sulfate and concentrated under reduced pressure until the product started to crystallize. To the residual solution was added dropwise over 30 min n-hexane. The resulting suspension was cooled to 2° C., stirred for 1 h and then filtered. The crystalline product was washed with n-hexane and dried to constant weight. (Z)-(RS)-(2-aminothiazol-4-yl)-[(tetrahydropyran-2-yloxyimino)]-acetic acid diethoxythio-phosphoryl ester was obtained as a white solid (28.01 g, yield=82%) and was stored under argon at -20° C. No further purificiation was necessary and the product was used as isolated for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05919939
Source datasetuspto-grants-1999_07
ORD IDord-5c9bfb6bca1a419b8f602c22cc702a3f
Source noteuspto-grants-1999_07