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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923672Generated: October 30, 2026

Potassium Hydroxide → 4-(1,3-Dimethyl-1H-pyrazolo[4,3-d]pyrimidin-7-yl)-6-((1-methylisoquinolin-6-yl)ethynyl)pyridin-2-amine

https://huagongshe.com/reaction/923672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactanttert-butyl-N-{1-[(4-{1,3-dimethyl-1H-pyrazolo[4,3-d]pyrimidin-7-yl}-6-[2-(1-methylisoquinolin-6-yl)ethynyl]pyridin-2-yl)carbamoyl]ethyl}-N-methylcarbamate H2HCID 178432658—
Product4-(1,3-Dimethyl-1H-pyrazolo[4,3-d]pyrimidin-7-yl)-6-((1-methylisoquinolin-6-yl)ethynyl)pyridin-2-amineHCID 117902868—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of tert-butyl-N-{1-[(4-{1,3-dimethyl-1H-pyrazolo[4,3-d]pyrimidin-7-yl}-6-[2-(1-methylisoquinolin-6-yl)ethynyl]pyridin-2-yl)carbamoyl]ethyl}-N-methylcarbamate H2 (150 mg, 0.31 mmol) and potassium hydroxide (1 mol/l solution in MeOH:water=2:1, 3 ml, 3 mmol) is stirred at 60° C. for 2 days. The precipitate is collected and purified by NP chromatography to yield 4-{1,3-dimethyl-1H-pyrazolo[4,3-d]pyrimidin-7-yl}-6-[2-(1-methylisoquinolin-6-yl)ethynyl]pyridin-2-amine. Yield: 110 mg (89%). HPLC-MS: M+H=406; tR=1.07 min (METHOD—1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278978B2
Source datasetuspto-grants-2016_03
ORD IDord-02f9d65122ee4fa4ae9371edbb91813e
Source noteuspto-grants-2016_03