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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726503Generated: November 1, 2026

Ethyl chloroformate → HCID 59656343, compound

https://huagongshe.com/reaction/1726503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantCarbonate IonHCID 19660—
ReactantHCID 66998005HCID 66998005—
SolventMethanolHCID 887—
ProductHCID 59656343HCID 59656343—

Reaction Conditions

Temperature25 °C

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 lh, 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. LC/MS showed m/z 407 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491827B2
Source datasetuspto-grants-2009_02
ORD IDord-a61859d8e8444ee287a9d5f596fb44bc
Source noteuspto-grants-2009_02