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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 639311Generated: October 27, 2026

Potassium Hydroxide → 6-Cyclopropylmethoxy-5-piperidin-1-yl-pyrazine-2-carboxylic acid

https://huagongshe.com/reaction/639311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantSodium hydrideHCID 24758—
ReactantCyclopropanemethanolHCID 75644—
Reactant6-Bromo-5-piperidin-1-yl-pyrazine-2-carboxylic acid methyl esterHCID 86619522—
SolventFormic AcidHCID 284—
SolventDimethylformamideHCID 6228—
Product6-Cyclopropylmethoxy-5-piperidin-1-yl-pyrazine-2-carboxylic acidHCID 6856799810%

Reaction Conditions

Temperature45 °C

Reaction Steps

A mixture of 0.12 g (0.4 mmol) 6-bromo-5-piperidin-1-yl-pyrazine-2-carboxylic acid methyl ester, 0.029 g (0.4 mmol) cyclopropyl methanol and 0.018 g (0.41 mmol) NaH (55% suspension in oil) in 2 mL DMF was shaken for an extended period of time. Afterwards, 0.1 mL KOH (5N aq.) was added and the mixture was heated to 45° C. for 1 h. After addition of formic acid the mixture was subjected to purification by preparative HPLC on reversed phase eluting with a gradient formed from acetonitrile, water and formic acid. The combined product fractions were evaporated to yield 11 mg (10%) of the title compound. m/z (ES+): 278.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691863B2
Source datasetuspto-grants-2010_04
ORD IDord-4d9434024e06406c94eb29c10e1a0e69
Source noteuspto-grants-2010_04