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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506800Generated: October 26, 2026

Potassium Hydroxide → HCID 68467161, compound

https://huagongshe.com/reaction/506800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactantcyclopropyl-[2-(5,6-dimethoxy-1-methyl-1H-pyrrolo[3,2-b]pyridin-3-yl)-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridin-4-ylmethyl]-amineHCID 68468463—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 68467161HCID 6846716196%

Reaction Steps

To a solution of 0.11 g of cyclopropyl-[2-(5,6-dimethoxy-1-methyl-1H-pyrrolo[3,2-b]pyridin-3-yl)-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridin-4-ylmethyl]amine in 20 cm3 of methanol, at a temperature in the region of 20° C., is added 1 cm3 of 5N potassium hydroxide. The reaction medium is refluxed for 24 hours. After cooling, the reaction medium is concentrated under reduced pressure. The residue obtained is taken up in 20 cm3 of water. The solid formed is filtered off on a sinter funnel. The solid obtained is taken up in 80 cm3 of dichloromethane and 3 cm3 of water. The organic phase is dried over magnesium sulfate, filtered and then concentrated under reduced pressure to give 0.075 g of cyclopropyl-[2-(5,6-dimethoxy-1-methyl-1H-pyrrolo[3,2-b]pyridin-3-yl)-1H-pyrrolo[2,3-b]pyridin-4-ylmethyl]amine with the following characteristics:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786114B2
Source datasetuspto-grants-2010_08
ORD IDord-9d43680dc2214d83953f383abd33923d
Source noteuspto-grants-2010_08