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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247296Generated: October 29, 2026

Hydrochloric Acid → N-(4,4-dimethyl-1,2,3,4-tetrahydro-isoquinolin-7-yl)-2-[(1H-pyrrolo[2,3-b]pyridin-4-ylmethyl)-amino]-nicotinamide

https://huagongshe.com/reaction/2247296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
Reactant4,4-dimethyl-7-({2-[(1H-pyrrolo[2,3-b]pyridin-4-ylmethyl)-amino]-pyridine-3-carbonyl}-amino)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl esterHCID 60053729—
Solvent1,4-DioxaneHCID 31275—
ProductN-(4,4-dimethyl-1,2,3,4-tetrahydro-isoquinolin-7-yl)-2-[(1H-pyrrolo[2,3-b]pyridin-4-ylmethyl)-amino]-nicotinamideHCID 10025493—

Reaction Steps

A mixture of 4,4-dimethyl-7-({2-[(1H-pyrrolo[2,3-b]pyridin-4-ylmethyl)-amino]-pyridine-3-carbonyl}-amino)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester (0.115 g, step A), HCl (4N, 3 mL) and dioxane (4 mL) was stirred at RT for overnight. Sat'd NaHCO3 was added until the bubbling stopped. The aqueous phase was extracted with EtOAc 3 times. The combined organic phases were dried over Na2SO4 and evaporated to yield a light purple oil as a crude product, which was purified by chromatography through silica gel (10 g, 5% MeOH/CHCl3 with 1% NH4OH) to afford N-(4,4-dimethyl-1,2,3,4-tetrahydro-isoquinolin-7-yl)-2-[(1H-pyrrolo[2,3-b]pyridin-4-ylmethyl)-amino]-nicotinamide. The material was further purified via silica gel column chromatography (10 g, 1% to 5% MeOH/CH2Cl2, stepwise gradient) to afford pure title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687643B2
Source datasetuspto-grants-2010_03
ORD IDord-16180ac8be0543e1a669b4d9d9eaa6ec
Source noteuspto-grants-2010_03