HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789355Generated: October 30, 2026
HCID 13768101, compound → N-diethylphosphoryl-2-{2-[2-(4-(3-fluorophenyl)piperazin-1-yl)ethyloxy]phenyl}thiazolidine-3-carbothioamide
https://huagongshe.com/reaction/1789355
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 13768101 | HCID 13768101 | — |
| Reactant | Diethylphosphoryl isothiocyanate | HCID 20188170 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-diethylphosphoryl-2-{2-[2-(4-(3-fluorophenyl)piperazin-1-yl)ethyloxy]phenyl}thiazolidine-3-carbothioamide | HCID 14095401 | 85.2% |
Reaction Steps
0.68 g of diethylphosphoryl isothiocyanate is added to a solution of 1.23 g of 2-{2-[2-(4-(3-fluorophenyl)piperazin-1-yl)ethyloxy]phenyl}thiazolidine in 20 ml of acetone, and the mixture is stirred for one day. The mixture is concentrated under reduced pressure to remove solvent. The residue is extracted with chloroform, and the extract is washed with a saturated sodium chloride solution, dried and concentrated under reduced pressure to remove solvent. The residue is purified by silica gel chromatography (solvent, chloroform:methanol=40:1), and the resultant product is recrystallized from ethyl acetate and ether. 1.49 g of N-diethylphosphoryl-2-{2-[2-(4-(3-fluorophenyl)piperazin-1-yl)ethyloxy]phenyl}thiazolidine-3-carbothioamide are obtained. Yield: 81%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04689327 |
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| Source dataset | uspto-grants-1987_08 |
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| ORD ID | ord-1bfbce77124b4ef7b75e6c9cc7cb718a |
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| Source note | uspto-grants-1987_08 |
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