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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990986Generated: October 30, 2026

Methylamine → N-methyl-4-(1,4-dihydroindeno[1,2-c]pyrazol-3-yl)benzamide

https://huagongshe.com/reaction/990986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantDiisopropylcarbodiimideHCID 12734—
Reactant4-PyrrolidinopyridineHCID 75567—
Reactant4-(1,4-Dihydroindeno[1,2-c]pyrazol-3-yl)benzoic acidHCID 18415847—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductN-methyl-4-(1,4-dihydroindeno[1,2-c]pyrazol-3-yl)benzamideHCID 18415900—

Reaction Steps

A mixture of 4-(1,4-dihydroindeno[1,2-c]pyrazol-3-yl)benzoic acid (0.8 g), methylamine in ethanol (0.27 ml of a 33% w/w solution), 4-pyrrolidinopyridine (0.47 g), diisopropylcarbodiimide (0.5 ml) and dichloromethane (30 ml) was stirred at ambient temperature for 20 hours. More methylamine in ethanol (0.3 ml of a 33% w/w solution), 4-pyrrolidinopyridine (0.5 g) and diisopropylcarbodiimide (1 ml) were added and the mixture was stirred for 3 hours at ambient temperature. The solvent was removed under reduced pressure at 50° C. The mixture was kept under vacuum for 2 hours and then dichloromethane (50 ml) was added. The mixture was stirred at ambient temperature for 20 hours and then allowed to stand for 72 hours. A solid was removed by filtration and purified by flash column chromatography on silica using toluene/acetic acid (10:1) and then ethyl acetate as the mobile phase to give N-methyl-4-(1,4-dihydroindeno[1,2-c]pyrazol-3-yl)benzamide, m.p. 182-188° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06462036B1
Source datasetuspto-grants-2002_10
ORD IDord-59a585b89f614855994b1a5eb3f4aef3
Source noteuspto-grants-2002_10