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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383053Generated: October 29, 2026

Sodium borohydride → HCID 67538376, compound

https://huagongshe.com/reaction/2383053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 67535969HCID 67535969—
SolventMethanolHCID 887—
ProductHCID 67538376HCID 67538376—

Reaction Steps

1-cyclohexyl-N-isobutyl-3,4-dihydroisoquinoline-7-carboxamide (689 mg) was dissolved in MeOH (12 mL). Sodium borohydride (100 mg) was added to the reaction mixture, followed by stirring at room temperature for 5 hours. The solvent was evaporated. To the resulting residue were added water and chloroform. The residue was extracted with chloroform and dried over magnesium sulfate. Then, the solvent was evaporated under reduced pressure to obtain 1-cyclohexyl-N-isobutyl-1,2,3,4-tetrahydroisoquinoline-7-carboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263607B2
Source datasetuspto-grants-2012_09
ORD IDord-80c26d920e0f4cd2bf3d275f284e6bed
Source noteuspto-grants-2012_09