HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27081Generated: October 31, 2026
Water → 2-(5-Chloropyrid-2-yl)-3-(4-ethoxycarbonylpiperazin-1-yl)carbonyloxy-isoindolin-1-one
https://huagongshe.com/reaction/27081
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Piperazinecarboxylic acid, ethyl ester, hydrochloride (1:1) | HCID 90438 | — |
| Reactant | 2-(5-Chloropyrid-2-yl)-3-phenoxycarbonyloxy-isoindolin-1-one | HCID 23343656 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(5-Chloropyrid-2-yl)-3-(4-ethoxycarbonylpiperazin-1-yl)carbonyloxy-isoindolin-1-one | HCID 13728649 | — |
Reaction Steps
Triethylamine (3.03 g.) is added to a suspension of 2-(5-chloropyrid-2-yl)-3-phenoxycarbonyloxy-isoindolin-1-one (3.8 g.) and 1-ethoxycarbonylpiperazine hydrochloride (4.86 g.) in acetonitrile (50 cc.), and the mixture is stirred for 18 hours at a temperature of about 20° C. Water (100 cc.) is then added and the insoluble product is filtered off and washed with water (10 cc.). After drying, a product (4 g.) is obtained which, after recrystallisation from acetonitrile (30 cc.), gives 2-(5-chloropyrid-2-yl)-3-(4-ethoxycarbonylpiperazin-1-yl)carbonyloxy-isoindolin-1-one (2.8 g.) melting at 160° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04220646 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-5f6592c6a4384358a914cfdad510b3b6 |
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| Source note | uspto-grants-1980_09 |
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