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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706218Generated: October 31, 2026

Sodium Hydroxide → 1-Cyano-4-methoxy-8-phenoxy-isoquinoline-3-carboxylic acid

https://huagongshe.com/reaction/706218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1-Cyano-4-methoxy-8-phenoxy-isoquinoline-3-carboxylic acid methyl esterHCID 67110488—
SolventMeOH tetrahydrofuranHCID 21899815—
Product1-Cyano-4-methoxy-8-phenoxy-isoquinoline-3-carboxylic acidHCID 6711012492.7%

Reaction Steps

To a mixture of 1-cyano-4-methoxy-8-phenoxy-isoquinoline-3-carboxylic acid methyl ester (727 mg, 2.18 mmol) and methanol/tetrahydrofuran (12.5 mL, 1:1.5) was added 2N sodium hydroxide (5.4 mL, 10.89 mmol) at room temperature. The yellow solution was stirred at that temperature for seventy minutes before it was concentrated. Water (20 mL) was added and the mixture was adjusted to pH=2 with 1N HCl (13 mL). The mixture was then extracted with dichloromethane and ethyl acetate. The combined organic layers were washed with brine, dried over anhydrous sodium sulfate, concentrated in vacuo to give the title compound as a yellow solid (647 mg): MS: (+) m/z 320.80 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174976B2
Source datasetuspto-grants-2015_11
ORD IDord-8114a5f0191d4d979dca22b5211cd701
Source noteuspto-grants-2015_11