HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476568Generated: October 30, 2026
1-(2-Hydroxyethyl)piperazine → HCID 14423121, compound
https://huagongshe.com/reaction/476568
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(2-Hydroxyethyl)piperazine | HCID 7677 | — |
| Reactant | HCID 14098030 | HCID 14098030 | — |
| Product | HCID 14423121 | HCID 14423121 | 40% |
Reaction Steps
A mixture of 6-chloro-1-methoxycarbonylmethyl-2-oxo-1,2-dihydrothiazolo[5,4-b]pyridine (10.32 g) and N-(2-hydroxyethyl)piperazine (10.4 g) was heated at 130° C. for 15 min. After cooling, the reaction mixture was poured into an ice-water. The precipitates obtained were extracted with chloroform. The chloroform layer was dried over magnesium sulfate, and evaporated to give crude material. The crude material was purified on a silica gel column chromatography using a mixture of methylene chloride and methanol (10:1). The desired fractions containing the objective compound were collected and evaporated. The crude crystals obtained were recrystallized from a mixture of methanol and diethyl ether to give 6-chloro-2-oxo-1-{[4-(2-hydroxyethyl)-1-piperazinyl]carbonylmethyl}-1,2-dihydrothiazolo[5,4-b]pyridine (5.70 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-84cac937ae724fc8944d076492b513b9 |
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| Source note | uspto-grants-1989_12 |
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