HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561324Generated: November 1, 2026
Ethyl chloroformate → HCID 59656343, compound
https://huagongshe.com/reaction/561324
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Carbonate Ion | HCID 19660 | — |
| Reactant | HCID 66998005 | HCID 66998005 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 59656343 | HCID 59656343 | — |
Reaction Steps
To a solution of 4-(1-hydroxy-ethyl)-naphthalene-1-sulfonic acid piperidin-4-ylamide acetic acid salt 37 (290 mg, 0.74 mmol) in MeOH (10 mL) was added MP-Carbonate (1.45 g, 3.69 mmol, 2.54 mmol/g). After shaking at 25° C. for 1 h, the solution was filtered. To the resultant solution was added ethyl chloroformate (120 mg, 1.11 mmol). After stirred for another 2 h at 25° C., the solution was concentrated in vacuo to give a solid. The crude material was purified by Flash column chromatography (CH2Cl2: MeOH) to provide 4-[4-(1-hydroxy-ethyl)-naphthalene-1-sulfonylamino]-piperidine-1-carboxylic acid ethyl ester 38. LCMS showed m/z 407 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063222B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-7d2c14be6a4d40889f3e700b1f186691 |
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| Source note | uspto-grants-2011_11 |
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