HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405357Generated: November 1, 2026
Ethyl chloroformate → HCID 68153433, compound
https://huagongshe.com/reaction/1405357
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1392466-65-7 | HCID 68153780 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 68153433 | HCID 68153433 | 63.2% |
Reaction Steps
Ethyl chloroformate (328.2 μL, 3.43 mmol) was added to a solution of tert-butyl spiro[3,4-dihydro-2H-pyrrolo[1,2-a]pyrazine-1,4′-piperidine]-1′-carboxylate (500 mg, 1.72 mmol) and K2CO3 (474.3 mg, 3.43 mmol) in acetonitrile (5.0 mL) and the reaction was stirred at room temperature overnight. The reaction was filtered using acetonitrile and the solvent was evaporated under reduced pressure. The compound was dissolved in ethyl acetate and washed with 1N hydrochloric acid and brine. The organic layer was dried over sodium sulfate, filtered, and concentrated under reduced pressure to yield 1-tert-butyl 2′-ethyl 3′,4′-dihydro-2′H-spiro[piperidine-4,1′-pyrrolo[1,2-a]pyrazine]-1,2′-dicarboxylate (395 mg, 63%) as an amber oil that was used in the next step without further purification. ESI-MS m/z calc. 363.2, found 364.3 (M+1)+; Retention time: 1.78 minutes (3 minute run).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916565B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-99224d72cf8e4f6b9d1165a198e9bbea |
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| Source note | uspto-grants-2014_12 |
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