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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261171Generated: October 31, 2026

p-Anisoyl chloride → HCID 66641274, compound

https://huagongshe.com/reaction/2261171

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
ReactantHCID 66641074HCID 66641074—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 66641274HCID 6664127471.7%

Reaction Steps

40 mg (0.233 mmoles) of 4-methoxy-benzoyl chloride in solution in 3 ml of dichloromethane is added to a mixture of 109 mg (0.233 mmoles) of tert-butyl 2-amino-3-{5-methyl-6-[4-(5,6,7,8-tetrahydro-[1,8]naphthyridin-2-yl)-piperidin-1-yl]-pyrimidin-4-ylamino}-propionate in solution in 6 ml of dichloromethane and 650 μl of pyridine. The reaction mixture is stirred at ambient temperature for 1 hour. Then, the solvent is evaporated off under reduced pressure (2 kPa) and the residue is chromatographed on silica gel with the following eluent: ethyl acetate-dichloromethane 50-50, ethyl acetate-dichloromethane/methanol (95/5) 50-50 then finishing with ethyl acetate-dichloromethane/methanol (9/1) 50-50. 98 mg of expected product is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846932B2
Source datasetuspto-grants-2010_12
ORD IDord-78bb04f12eb6439a90a479bec3493ee0
Source noteuspto-grants-2010_12