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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409286Generated: October 29, 2026

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

https://huagongshe.com/reaction/409286

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 numberUS08759373B2
Source datasetuspto-grants-2014_06
ORD IDord-108f535862594c3da108cecd4e0267b8
Source noteuspto-grants-2014_06