HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114732Generated: October 31, 2026
Methanesulfonyl chloride → HCID 86591982, compound
https://huagongshe.com/reaction/2114732
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 54107592 | HCID 54107592 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 86591982 | HCID 86591982 | 13% |
Reaction Steps
To a solution containing 2-(4-fluorophenyl)-1-{4-[(2-piperidyl)ethoxy]benzyl}-1,2,3,4-tetrahydroisoquinolin-6-ol (0.100 g, 0.2 mmol) in pyridine (0.4 ml) was added methyl sulfonyl chloride (25 μl, 0.32 mmol). After stirring for five hours, solvent was removed and the reaction was basified with aqueous sodium bicarbonate solution. The reaction was extracted with dichloromethane and concentrated. The product was purified by semipreparative HLPC (C-18 column, 10-100% acetonitrile/water with 0.1% trifluoroacetic acid). The acetonitrile was removed from the HPLC fractions containing the desired product. Ethyl acetate was added and the solution neutralized using saturated sodium bicarbonate. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated to provide the title compound (0.0135 g, 13% yield): 1H NMR (CDCl3) 6.7-7.1 (m, 11H), 4.78 (t, 1H), 4.1 (t, 3H), 3.45-3.62 (m, 2H), 2.62-3.18 (m, 8H), 2.58 (m, 4H), 1.63 (m, 4H), 1.43 (m, 2H); ES-MS (m/z) 539 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07435729B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-2e6381a5d5294f5698099e1e3c951574 |
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| Source note | uspto-grants-2008_10 |
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