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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374035Generated: October 30, 2026

Acetyl chloride → HCID 59853014, compound

https://huagongshe.com/reaction/2374035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantHCID 59852856HCID 59852856—
CatalystAcetyl chlorideHCID 6367—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductHCID 59853014HCID 59853014132.6%

Reaction Steps

A tert-butyl 4-(2-aminopyridin-4-yloxy)-3-fluorophenylcarbamate (150 mg, 0.47 mmol) in anhydrous pyridine (0.5 mL) was cooled to 10° C. and treated with acetyl chloride (33 μL, 0.47 nmol) and the mixture stirred for 45 min. An additional portion of acetyl chloride (16 μL, 0.24 mmol) was added to the reaction and stirring continued for 25 min. The mixture was diluted with EtOAc (20 mL), washed with brine, dried (MgSO4) and concentrated under vacuum to give the title compound (115 mg, 68%). 1H NMR (DMSO-d6) δ 10.55 (s, 1H), 9.71 (s, 1H), 8.16 (d, 1H, J=5.5 Hz), 7.63-7.55 (m, 2H), 7.29-7.23 (m, 2H), 6.68-6.63 (m, 1H), 2.02 (s, 3H), 1.48 (s, 9H); MS(ESI+): m/z 362.22 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459562B2
Source datasetuspto-grants-2008_12
ORD IDord-0fd34364894946ce9d33cf8452d2b69e
Source noteuspto-grants-2008_12