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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766025Generated: November 1, 2026

Succinic Acid → HCID 21108213, compound

https://huagongshe.com/reaction/1766025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSuccinic AcidHCID 1110—
ReactantTriethylamineHCID 8471—
Reactant1-Naphthalenesulfonyl chlorideHCID 66560—
ReactantHCID 17848893HCID 17848893—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 21108213HCID 21108213—

Reaction Steps

A solution of 1-naphthalenesulfonyl chloride (388 mg, 1.72 mmol) in acetonitrile (5 ml) was added to a solution of 3,4-dihydro-6-[2-(N,N-propylamino)ethyl]-2H-1,4-benzoxazine hydrochloride (300 mg, 1.14 mmol) obtained in Example 134, 4-dimethylaminopyridine (140 mg, 1.14 mmol) and triethylamine (0.48 ml, 3.43 mmol) in acetonitrile (15 ml) under cooling with ice-bath, and the mixture was stirred at room temperature for 4 hours. Water (50 ml) was added to the reaction solution which was then extracted with ethyl acetate. The extract was washed with 10% aqueous potassium carbonate and a saturated saline solution, dried over anhydrous sodium sulfate and concentrated. The residues were purified by silica gel column chromatography (developing solvent; ethyl acetate), and succinic acid (1 equivalent) was added thereto, and the product was recrystallized from ethyl acetate-diisopropyl ether, whereby the title compound (220 mg) was obtained as crystals with a mp of 144 to 145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07229986B2
Source datasetuspto-grants-2007_06
ORD IDord-13b92da7f00a4b44ad8d7e63d5084369
Source noteuspto-grants-2007_06