Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670286Generated: October 31, 2026

Acetyl chloride → HCID 59853014, compound

https://huagongshe.com/reaction/1670286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantHCID 59852856HCID 59852856—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductHCID 59853014HCID 5985301468%

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 mmol) 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 numberUS07989477B2
Source datasetuspto-grants-2011_08
ORD IDord-20863772e44a47d78b9e8a7c9cb3e350
Source noteuspto-grants-2011_08