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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215148Generated: October 31, 2026

p-Toluenesulfonic acid → HCID 86587140, compound

https://huagongshe.com/reaction/2215148

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2,5-HexanedioneHCID 8035—
Reactant(4-amino-3-methoxy-phenyl)[10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-10-yl]methanoneHCID 10806563—
SolventBenzeneHCID 241—
SolventDichloromethaneHCID 6344—
ProductHCID 86587140HCID 86587140—

Reaction Steps

A solution of (4-amino-3-methoxy-phenyl)[10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-10-yl]methanone prepared in the manner of Albright et al., E.P.636625-A2 (0.675g, 2 mmol) and acetonyl acetone (0.3 mL, 2.5 mmol) in benzene (100 mL) was treated with a crystal of para-toluenesulfonic acid. The stirred solution was warmed to reflux for 46 hrs using a Dean Stark trap. The reaction was cooled to room temperature, diluted with dichloromethane (100 mL), washed with saturated aqueous sodium bicarbonate then water. The residue (oil, 0.900 g) was flash chromatography on silica gel eluting with 20% ethyl acetate in hexane to yield 0.610 g of the title compound as a white foam. Recrystallization of a sample of this material yielded yellow crystals, m.p. 141–144° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109193B2
Source datasetuspto-grants-2006_09
ORD IDord-2e785dd9066c4ef082ceadbbb9dc509c
Source noteuspto-grants-2006_09