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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491164Generated: October 27, 2026

4-Nitrophenyl chloroformate → HCID 68676084, compound

https://huagongshe.com/reaction/491164

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrophenyl chloroformateHCID 82129—
Reactant3-Piperidin-4-yl-1,3-dihydroimidazo[4,5-c]quinolin-2-oneHCID 18321559—
ReactantHCID 67273374HCID 67273374—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
ProductHCID 68676084HCID 68676084—

Reaction Steps

Under a nitrogen atmosphere 1.28 g (6.36 mmol) 4-nitrophenyl chloroformate were added at RT to a solution of 0.78 g (6.36 mmol) 4-dimethylaminopyridine in 100 mL pyridine and the mixture was stirred for 1 h at RT. Then a solution of 2.00 g (6.36 mmol) methyl(R)-3-(4-benzyloxy-3,5-dimethyl-phenyl)-2-hydroxy-propionate in 20 mL pyridine was added dropwise at RT and the reaction mixture was stirred for 2 h after the end of the addition. Then 1.71 g (6.36 mmol) 3-piperidin-4-yl-1,3-dihydro-imidazo[4,5-c]quinoline-2-one was added to the reaction mixture, which was then heated to 100° C. for 4 h. The precipitate formed was filtered off, the filtrate was evaporated down i.vac., the residue was mixed with 200 mL EtOAc and 200 mL semisaturated KHSO4 solution, the product being obtained as a precipitate. This was suction filtered and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528129B2
Source datasetuspto-grants-2009_05
ORD IDord-cf8ca54028a64660bc5dceb41eab9d86
Source noteuspto-grants-2009_05