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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523842Generated: October 26, 2026

Potassium Carbonate → 1-Dimethylaminomethyl-4-hydroxy-7-phenylsulfanyl-isoquinoline-3-carboxylic acid butyl ester

https://huagongshe.com/reaction/523842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN,N-dimethylmethyleneammoniumiodideHCID 21892197—
Reactant4-Hydroxy-7-phenylsulfanyl-isoquinoline-3-carboxylic acid butyl esterHCID 66713092—
SolventDichloromethaneHCID 6344—
Product1-Dimethylaminomethyl-4-hydroxy-7-phenylsulfanyl-isoquinoline-3-carboxylic acid butyl esterHCID 6671317316.6%

Reaction Steps

A mixture of 4-Hydroxy-7-phenylsulfanyl-isoquinoline-3-carboxylic acid butyl ester (177 mg, 0.5 mmol; see example D-1f), N,N-dimethylmethyleneammonium iodide (94 mg, 0.5 mmol), K2CO3 (104 mg, 0.75 mmol), and anhydrous CH2Cl2 (3 ml) was stirred at ambient temperature for 2.5 d before the mixture was concentrated in vacuo. To the residue was added water (15 ml), the mixture was acidified by addition of 6N HCl and then washed with Et2O (3×30 ml). Subsequently, the mixture was neutralized by the addition of concentrated aqueous NaHCO3 and extracted with EtOAc (20 ml). The organic phase was dried over MgSO4 and concentrated in vacuo to give the title compound as a dark oil (34 mg); MS-(+)-ion M+1=411.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09339527B2
Source datasetuspto-grants-2016_05
ORD IDord-b07bf909f97d4f8cbf3d788e17f81e24
Source noteuspto-grants-2016_05