HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581230Generated: October 30, 2026
Dabco → O-[(2Z)-2-[(Acetyloxy)imino]-2-(2-amino-1,3-thiazol-4-yl)acetyl] O,O-diethyl phosphorothioate
https://huagongshe.com/reaction/581230
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dabco | HCID 9237 | — |
| Reactant | O,O-diethyl phosphorochloridothioate | HCID 17305 | — |
| Reactant | HCID 88204478 | HCID 88204478 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | O-[(2Z)-2-[(Acetyloxy)imino]-2-(2-amino-1,3-thiazol-4-yl)acetyl] O,O-diethyl phosphorothioate | HCID 15435118 | 86% |
Reaction Steps
To a stirred solution of 134.9 g (Z)-(2-aminothiazol4-yl)-acetoxyiminoacetic acid dihydrate (508.6 mmol) and 570 mg 1,4-diazabicyclo[2.2.2]octane (DABCO) (5.09 mmol) in 1500 ml dimethylacetamide was added under argon 158 ml tributylamine (661 mmol). The yellowish solution was cooled to -20° C. and over 30 min was added dropwise 104 ml diethyl chlorothiophosphate (661 mmol). Stirring was continued at -20° C. for 3.5 h. The reaction was followed by HPLC. After 3 h, all starting material was consumed. The reaction mixture was allowed to warm up to 0° C. and over 1.0 h was added dropwise 2200 ml water. The precipitated product was filtered, washed with water and dissolved in 800 ml dichloromethane. The aqueous layer was back-extracted with 300 ml dichloromethane. The combined organic layers were dried over 70 g sodium sulfate and concentrated under reduced pressure until the product started to crystallize. The residual solution was cooled to 2° C. and 1200 ml n-hexane was added dropwise over 1 h. The resulting suspension was stirred for 1 h at 2° C. and then filtered. The crystalline product was washed with n-hexane and dried to constant weight. (Z)-(2-aminothiazol-4-yl)-acetoxyiminoacetic acid diethoxythiophosphoryl ester was obtained as a white solid (166.9 g, yield=86%, mp 128-130° C. and was stored under argon at -20° C. No further purification was necessary and the product was used as isolated for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05919939 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-1324ccca96aa4321a09b34ff37c4fcdf |
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| Source note | uspto-grants-1999_07 |
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