HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073178Generated: October 30, 2026
1-Chloroethyl chloroformate → HCID 14850201, compound
https://huagongshe.com/reaction/2073178
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | HCID 14850200 | HCID 14850200 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 14850201 | HCID 14850201 | 72.6% |
Reaction Steps
A solution of 1-chloroethyl chloroformate (9.7ml, 90 mmol) in 1,2-dichloroethane (25ml) was added to an ice-chilled solution of N-(2-pyrazinyl)-N-(1-phenylmethyl-4-piperidinyl)-2-furanamide (45 mmol) and 1,2-dichloroethane (125ml). The reaction mixture was stirred under reflux for 5 hours, then cooled and concentrated under vacuum. The crude carbamate residue was dissolved in methanol (150ml) and the reaction solution was heated under reflux for 2 hours. The reaction solution was cooled, decolorizing carbon (10g, Darco G-60) was added to the mixture, then the suspension was heated and stirred under reflux for 15 minutes. The suspension was filtered through Celite and the filtrate was concentrated under vacuum. The residue was suspended in hot isopropanol (100ml), then cooled and filtered. The pale maize colored powder was dried under vacuum (85° C., 0.01mm Hg, 2 hours) to yield N-(2-pyrazinyl)-N-(4piperidinyl)-2-furanamide (8.9g, 72%) as the hydrochloride salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04916142 |
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| Source dataset | uspto-grants-1990_04 |
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| ORD ID | ord-22a05c2ebee44308853d3486e16b6c30 |
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| Source note | uspto-grants-1990_04 |
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