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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242072Generated: October 30, 2026

Hydrochloric Acid → HCID 66869221, compound

https://huagongshe.com/reaction/242072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBoraneHCID 6331—
ReactantHCID 86653001HCID 86653001—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66869221HCID 66869221—

Reaction Conditions

Temperature0 °C

Reaction Steps

N-[2-({1-[1-(4-Fluorophenyl)cyclobutyl]-2-(trifluoroacetyl)-1,2,3,4-tetrahydroisoquinolin-7-yl}oxy)ethyl]propane-1-sulfonamide (49 mg, 0.09 mmol) was dissolved in dry tetrahydrofuran (0.6 mL) under an atmosphere of nitrogen. The solution was cooled to 0° C. and a 1M solution of borane in tetrahydrofuran (0.181 mL, 0.181 mmol) was added dropwise. The reaction mixture was warmed to room temperature and then heated under reflux for 2 h. The solvent was evaporated in vacuo, the residue was dissolved in dichloromethane (20 mL) and washed with water (10 mL). The organic layer was dried (MgSO4) and concentrated in vacuo. The product was dissolved in dichloromethane (2 mL) and treated with 5N isopropanolic hydrochloric acid (27 μL, 0.135 mmol). The solvents were evaporated and the product was dried in vacuo. Yield: 45 mg (0.08 mmol, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653100B2
Source datasetuspto-grants-2014_02
ORD IDord-a91f1fcd6793468daac1d92ac20c424e
Source noteuspto-grants-2014_02