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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643157Generated: October 29, 2026

4-Nitrophenyl chloroformate → HCID 68676170, compound

https://huagongshe.com/reaction/643157

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrophenyl chloroformateHCID 82129—
Reactant3-(Piperidin-4-yl)quinolin-2(1H)-oneHCID 18321046—
Reactantmethyl(R)-3-(4-benzyloxy-3,5-dimethyl-phenyl)-2-hydroxy-propionateHCID 67273374—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68676170HCID 68676170—

Reaction Conditions

Temperature60 °C

Reaction Steps

Under a nitrogen atmosphere 0.91 g (4.38 mmol) 4-nitrophenyl chloroformate in 10 mL THF were metered into 20 mL pyridine within 10 min at a bath temperature of 60° C., the mixture was stirred for 10 min, then 1.38 g (4.38 mmol) methyl (R)-3-(4-benzyloxy-3,5-dimethyl-phenyl)-2-hydroxy-propionate in 40 mL pyridine were added and the reaction mixture was stirred for 2 h at 60° C. The reaction solution was combined with 1.00 g (4.38 mmol) 3-piperidin-4-yl-1H-quinoline-2-one and stirred for 4 h at 100° C. The reaction mixture was evaporated down i.vac. and the residue was purified by HPLC. The fractions containing the product were combined, evaporated down i.vac., the residue was made alkaline with 15% K2CO3 solution, the precipitate was suction filtered, washed with 20 mL water and dried at 50° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696209B2
Source datasetuspto-grants-2010_04
ORD IDord-33b6433eecfa485e980b6ae881251536
Source noteuspto-grants-2010_04