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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710254Generated: October 29, 2026

4-Fluorobenzoyl chloride → HCID 89690731, compound

https://huagongshe.com/reaction/710254

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzoyl chlorideHCID 67879—
ReactantHCID 89690720HCID 89690720—
SolventPyridineHCID 1049—
ProductHCID 89690731HCID 8969073167.3%

Reaction Conditions

Temperature-5 °C

Reaction Steps

Tert-butyl 2-(3-amino-1H-indazol-6-yl)morpholine-4-carboxylate (43 mg, 0.135 mmol) was dissolved in pyridine (0.2 ml) and the solution was cooled to −5° C. 4-fluorobenzoyl chloride (21.4 mg, 0.135 mmo) was slowly added. After 5 min, the cooling bath was removed and stirring was continuing overnight. The reaction mixture was diluted with ethylacetate (2 ml) and washed with 1M citric acid solution (2 ml). The organic layer was dried over MgSO4 and concentrated in vacuo to give a brown oil which was further purified by flash column chromatography (silica gel, 50% to 100% ethyl acetate in heptane). The product was isolated as a yellow solid (40 mg, 67%), MS (ISP): 441.3 (100%, ([M-tBu+H]+), 385.2 (38%, [M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181230B2
Source datasetuspto-grants-2015_11
ORD IDord-8f0cb09a32944b7aa7787d88b1dedb8d
Source noteuspto-grants-2015_11