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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387675Generated: October 30, 2026

Sodium Bicarbonate → HCID 68473665, compound

https://huagongshe.com/reaction/387675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 68473018HCID 68473018—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 68473665HCID 68473665—

Reaction Conditions

Temperature150 °C

Reaction Steps

Added to a solution of 0.4 g of methyl 7-bromo-1-oxo-2-(1-propylbutyl)-1,2,3,4-tetrahydroisoquinoline-5-carboxylate in 12.5 cm3 of dioxane and 2.5 cm3 of water, at a temperature close to 20° C., are 196 mg of sodium bicarbonate. The reaction medium is then degassed under an argon atmosphere, then 147.5 mg of 2-cyanophenylboronic acid and 96 mg of tetrakis(triphenylphosphine)palladium are added. The mixture is heated at 150° C. in a microwave oven for 4 minutes, cooled to a temperature close to 20° C. and filtered. The filtrate is taken up by 20 cm3 of dichloromethane and 20 cm3 of water. The organic phase is extracted, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure (5 kPa). The residual solution (around 3 cm3) is purified by flash chromatography over silica (column: 50 g; spherical silica of BP-SUP type, partical size: 20-40 μm; eluent: 80% heptane/20% ethyl acetate then 60% heptane/40% ethyl acetate then 50% heptane/50% ethyl acetate). After concentrating the fractions under reduced pressure, 178 mg of methyl 7-(2-cyanophenyl)-1-oxo-2-(1-propylbutyl)-1,2,3,4-tetrahydroisoquinoline-5-carboxylate are obtained in the form of a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372864B2
Source datasetuspto-grants-2013_02
ORD IDord-a557dfc091dd4c05874c3d6ef605f29f
Source noteuspto-grants-2013_02