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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374009Generated: October 28, 2026

Chloroacetyl chloride → HCID 59853068, compound

https://huagongshe.com/reaction/2374009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
Reactant2-PyrrolidoneHCID 12025—
Reactant2-Propyn-1-amine, 3-[4-(2-fluoro-4-nitrophenoxy)-3-pyridinyl]-HCID 59852907—
SolventDichloromethaneHCID 6344—
ProductHCID 59853068HCID 5985306839%

Reaction Steps

A solution of 3-(4-(2-fluoro-4-nitrophenoxy)pyridin-3-yl)prop-2-yn-1-amine (80 mg, 0.26 mmol) in anhydrous CH2Cl2 (2.5 mL) was cooled to 0° C. and treated with chloroacetyl chloride (40 mg, 0.37 mmol) the mixture was stirred at rt for 1 h. The mixture was concentrated under vacuum to removed the solvent and excess reagent and the residue redissolved in CH3CN (1.5 mL), treated with pyrrolidone (55 mg, 0.78 mmol) and stirred at rt for 4 h. The mixture was partitioned between EtOAc and saturated aq. NaHCO3 solution and the organic phase separated, washed with brine, dried (MgSO4) and concentrated to give crude product. The residue was purified by flash chromatography on silica gel eluting with 0-10% MeOH/CH2Cl2 to afford the title compound (40 mg, 39%) as a brown oil. 1H NMR (DMSO-d6) δ 8.66 (s, 1H), 8.50 (d, 1H, J=6.1 Hz), 8.41 (dd, 1H, J=2.8, 10.4 Hz), 8.18-8.15 (m, 2H), 7.51 (dd, 1H, J=8.3, 8.8 Hz), 7.06 (d, 1H, J=5.5 Hz) 4.10 (d, 2H, J=5.5 Hz), 3.01 (s, 2H), 2.47-2.43 (m, 4H), 1.67-1.63 (m, 4H); MS(ESI+): m/z 399.27 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459562B2
Source datasetuspto-grants-2008_12
ORD IDord-051d4c44d19541c38350a970ceb26984
Source noteuspto-grants-2008_12