HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242072Generated: October 30, 2026
Hydrochloric Acid → HCID 66869221, compound
https://huagongshe.com/reaction/242072
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Borane | HCID 6331 | — |
| Reactant | HCID 86653001 | HCID 86653001 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66869221 | HCID 66869221 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653100B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-a91f1fcd6793468daac1d92ac20c424e |
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| Source note | uspto-grants-2014_02 |
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