HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476571Generated: October 30, 2026
Acetic Anhydride → HCID 14423126, compound
https://huagongshe.com/reaction/476571
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 14423121 | HCID 14423121 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 14423126 | HCID 14423126 | 79.5% |
Reaction Steps
To an ice-cooled solution of 6-chloro-2-oxo-1-{[4-(2-hydroxyethyl)-1-piperazinyl]carbonylmethyl]-1,2-dihydrothiazolo[5,4-b]pyridine (1.35 g) in dry pyridine (10 ml), acetic anhydride (0.73 g) was added dropwise and then the mixture was stirred at the temperature for 2 hours and at the room temperature for 4 hours. After removal of the solvent, the residual oil obtained was purified on an aluminum-oxide column chromatography using a mixture of chloroform and n-hexane (2:1). The fractions containing the objective compound were collected and evaporated to give crude crystals. The crude crystals were recrystallized from ethyl acetate to afford 6-chloro-2-oxo-1-{[4-(2-acetoxyethyl)-1-piperazinyl]carbonylmethyl}-1,2-dihydrothiazolo[5,4-b]pyridine (1,2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04885297 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-aa805ceb73cf4fb68a4d6823a736590d |
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| Source note | uspto-grants-1989_12 |
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