HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648590Generated: October 27, 2026
Phosphorus trichloride → 2-Amino-5-(4-pyridyl)-4-[(4-piperonyl-1-piperazinyl)carbonyl]thiazole
https://huagongshe.com/reaction/648590
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | 1-Piperonylpiperazine | HCID 94426 | — |
| Reactant | 2-Amino-5-(pyridin-4-yl)-1,3-thiazole-4-carboxylic acid | HCID 20144986 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-Amino-5-(4-pyridyl)-4-[(4-piperonyl-1-piperazinyl)carbonyl]thiazole | HCID 20145081 | 19% |
Reaction Steps
To a mixture of 1-piperonylpiperazine (2.72 g) and phosphorus trichloride (0.49 ml) in pyridine (20 ml) was added 2-amino-5-(4-pyridyl)-4-thiazolecarboxylic acid (1.24 g) and the mixture was stirred at 80° C. for 3 hours. The reaction mixture was evaporated in vacuo and the residue was dissolved in a mixture of ethyl acetate and water. The resultant mixture was adjusted to pH 8.0 with saturated aqueous potassium carbonate. The organic extract was dried over magnesium sulfate. The solvent was evaporated in vacuo to give a crystalline residue, which was recrystallized from ethyl acetate to afford 2-amino-5-(4-pyridyl)-4-[(4-piperonyl-1-piperazinyl)carbonyl]thiazole (0.45 g). mp 216°-217° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04735957 |
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| Source dataset | uspto-grants-1988_04 |
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| ORD ID | ord-1fb820e14d0449cf8bd37a69fee45a8d |
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| Source note | uspto-grants-1988_04 |
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