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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730410Generated: October 31, 2026

Hydrochloric Acid → HCID 69058882, compound

https://huagongshe.com/reaction/730410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTolueneHCID 1140—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 86606792HCID 86606792—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69058882HCID 6905888292%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of ethyl (E)-3-[3-cyano-4,6-dimethyl-1-(1,2,3,4-tetrahydro-1-naphthalenyl)-1H-pyrrolo[2,3-b]pyridin-2-yl]-2-propenoate (1.2 g, 3 mmol) in tetrahydrofuran (6 ml)-toluene (6 ml) was heated to 50° C. To the resultant solution was added a 2 N aqueous sodium hydroxide solution (4 ml, 8 mmol) and the mixture was stirred at 50° C. for 20 minutes. Then, water (100 ml) was added to the reaction mixture, which was adjusted to pH 3 to 4 with 12 N hydrochloric acid, and then the product was extracted using ethyl acetate-tetrahydrofuran (3:1, v/v). The organic extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and the solvent was removed under vacuum. Hexane was added to the residue on a solid material and the residue was finely crushed using a spatula. The solid was collected by filtration using Kiriyama Roht and was washed with hexane to give the title compound (yield (amount) 1.0 g, yield (rate) 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582651B2
Source datasetuspto-grants-2009_09
ORD IDord-72e2be67fa7b4d389c81634a77b90de2
Source noteuspto-grants-2009_09