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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934992Generated: October 30, 2026

4-Methylmorpholine → HCID 22466693, compound

https://huagongshe.com/reaction/1934992

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 578964HCID 578964—
ReactantHCID 22466726HCID 22466726—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22466693HCID 22466693—

Reaction Conditions

Temperature0 °C

Reaction Steps

Partially dissolved 1.21 (7.22 mmol) 4-piperidino-2-butynoic acid in 100 ml THF and chilled to 0° C. under N2. Added 955 μl (8.67 mmol) N-methylmorpholine and 750 μl (5.78 mmol) isobutyl chloroformate. Stirred for 40 minutes and added a solution of 840 mg (2.89 mmol) 6-amino-4-[(3-methoxyphenyl)amino]-3-quinolinecarbonitrile dissolved in 10 ml hot pyridine. At 2 hours, poured into ice water and made basic with saturated sodium bicarbonate. Extracted with ethyl acetate, dried with sodium sulfate, and stripped down to a small volume, which was loaded onto a column of silica gel. Eluted with 10% methanol/ethyl acetate, stripped solvent of desired fractions, and dried in vacuo, giving 970 mg of green solid: mass spectrum (electrospray m/e): M+H=440.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384051B1
Source datasetuspto-grants-2002_05
ORD IDord-4552a9f5bede45faab090a5b77891c00
Source noteuspto-grants-2002_05