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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732040Generated: October 30, 2026

Triethylamine → HCID 13746892, compound

https://huagongshe.com/reaction/1732040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant5-Mesyl-o-anisic acidHCID 170840—
Reactant1,2-Diethyl-4-pyrazolidinamineHCID 559199—
SolventDichloromethaneHCID 6344—
ProductHCID 13746892HCID 13746892109.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

Triethylamine (1.01 g, 0.010 mole) was added to a stirred mixture of 5-methylsulfonyl-2-methoxybenzoic acid (2.30 g, 0.010 mole) in 50 ml of methylene chloride. The mixture was cooled to 0° C. for 20 minutes and maintained at this temperature while ethyl chloroformate (1.09 g, 0.010 mole) was added dropwise. After another 20 minutes of stirring at 0° C., a solution of 1,2-diethyl-4-aminopyrazolidine (2.43 g, 0.010 mole) in 10 l of methylene chloride was added dropwise. The reaction mixture was allowed to come to ambient temperature and was stirred for 18 hrs. The reaction mixture was then extracted with 10% sodium bicarbonate solution, the methylene chloride layer separated and dried over magnesium sulfate. The methylene chloride solution was concentrated to give 3.90 g of a tanbrown solid which was recrystallized from water. A sulfate salt was prepared which was converted back to the free base. The solid free base that formed was recrystallized from ethanol-isopropyl ether to give 1.03 g (29%) of title compound; m.p. 123°-124° C. The compound was vacuum dried at 110° C.; the melting point was unchanged.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04624961
Source datasetuspto-grants-1986_11
ORD IDord-2c93560398f644b29a6abdb95ff1479e
Source noteuspto-grants-1986_11