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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424138Generated: October 29, 2026

Acetyl chloride → HCID 24999449, compound

https://huagongshe.com/reaction/424138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantHCID 24829325HCID 24829325—
SolventDichloromethaneHCID 6344—
ProductHCID 24999449HCID 2499944930%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° C. solution of example 1, (4-{4-[({3-tert-butyl-1-[3-(hydroxymethyl)phenyl]-1H-pyrazol-5-yl}carbamoyl)amino]-3-fluorophenoxy}-N-methylpyridine-2-carboxamide, (1.00 g, 1.88 mmol) in dichloromethane (15 mL) was added dropwise acetyl chloride (0.15 mL, 2.07 mmol). The reaction mixture was allowed to stir at 0° C. for 1 h. The reaction mixture was quenched with water and extracted with CH2Cl2. The combined organic layer was dried and concentrated. The crude material was purified via column chromatography (CH2Cl2:2M NH3 in MeOH, 97:3) to afford 0.32 g (30%) of the desired product as a white powder. MS m/z 575.1 (M+H)+; Retention time (LC-MS): 3.55 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101773B2
Source datasetuspto-grants-2012_01
ORD IDord-acca914e7b1e453d9ccf3a7bc3101d3d
Source noteuspto-grants-2012_01