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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735247Generated: October 31, 2026

Triethylamine → HCID 18917511, compound

https://huagongshe.com/reaction/1735247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5,10-dihydro-4H-pyrazolo[5,1-c][1,4]benzodiazepineHCID 13062825—
Reactant6-(5-Fluoro-2-methylbenzoyl)aminopyridine-3-carbonyl chlorideHCID 15508250—
SolventDichloromethaneHCID 6344—
ProductHCID 18917511HCID 1891751177.1%

Reaction Steps

To a chilled (0° C.) solution of 0.37 g of 5,10-dihydro-4H-pyrazolo[5, 1-c][1,4]benzodiazepine and 836 microliters of triethylamine in 5 ml of dichloromethane is added 0.761 g of 6-[(5-fluoro-2-methylbenzoyl)amino]pyridine-3-carbonyl chloride. The mixture is stirred at room temperature under argon for 5 hours. An additional 420 microliners of triethylamine and 0.38 g of 6-[(5-fluoro-2-methylbenzoyl)amino]pyridine-3-carbonyl chloride is added and the mixture stirred 16 hours. The mixture is diluted with 60 ml of dichloromethane and washed with 25 ml each of H2O, 1M NaHCO3, brine and dried (Na2SO4). The solution is filtered (twice) through a thin pad of hydrous magnesium silicate and the pad washed with dichloromethane. The filtrate is concentrated to give a yellow glass (0.68 g) which is crystallized from ethyl acetate to give 0.38 g of white crystals, m.p. 250° -260° C.; mass spectrum (FABL) 442.4 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05536718
Source datasetuspto-grants-1996_07
ORD IDord-6ba322a0654e445799b12ed655094790
Source noteuspto-grants-1996_07