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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242105Generated: November 1, 2026

Sodium borohydride → HCID 86653007, compound

https://huagongshe.com/reaction/242105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86653006HCID 86653006—
SolventMethanolHCID 887—
ProductHCID 86653007HCID 86653007—

Reaction Steps

N-[2-({1-[1-(6-Chloropyridin-2-yl)cyclobutyl]-3,4-dihydroisoquinolin-7-yl}oxy)ethyl]propane-1-sulfonamide (36 mg, 0.78 mmol) was dissolved in methanol (1 ml). Sodiumborohydride (12 mg, 0.31 mmol) was added and stirring was continued at room temperature over night. The solvent was evaporated in vacuo and the residue partitioned between dichloromethane and 1N aqueous sodium hydroxide solution. The layers were separated and the organic layer was dried (MgSO4) and concentrated in vacuo. The crude product was used for the next step without further purification. Yield: 9 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653100B2
Source datasetuspto-grants-2014_02
ORD IDord-667cd085baa24d44ba289116fdbf151d
Source noteuspto-grants-2014_02