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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953464Generated: October 25, 2026

4-Methylmorpholine → HCID 23298253, compound

https://huagongshe.com/reaction/1953464

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1-Cyclobutylmethanamine hydrochlorideHCID 21707944—
Reactant4-Chlorosulfonyl-3-(N,N-di-t-butoxycarbonylamino)-1-ethyloxycarbonylmethyl-2-pyridinoneHCID 23298250—
SolventDichloromethaneHCID 6344—
ProductHCID 23298253HCID 23298253—

Reaction Steps

NMM (1.43 mL, 13.0 mmol) was added to a stirred mixture of 4-chlorosulfonyl-3-(N,N-di-t-butoxycarbonylamino)-1-ethyloxycarbonylmethyl-2-pyridinone (as a mixture from Step H, 0.84 g) and cyclobutylmethylamine hydrochloride (348 mg, 2.86 mmol) in methylene chloride (15 mL). After 16 h the reaction was diluted with methylene chloride and washed with 10% citric acid solution. The organic layer was dried (Na2SO4) and evaporated. The residue was purified by flash column chromatography on silica (40% ethyl acetate/hexanes). HCl gas was bubbled through a stirred solution of the resulting compound in ethyl acetate (10 mL) at 0° C. for 15 min. The reaction was warmed to rt and after a further 3 h it was evaporated to give the title compound as a solid;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06117888
Source datasetuspto-grants-2000_09
ORD IDord-c9880aa6f3674fa69b86f03a7c17fc6d
Source noteuspto-grants-2000_09