HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427816Generated: November 4, 2026
5,6,7,8-Tetrahydro-2-naphthol → HCID 72545673, compound
https://huagongshe.com/reaction/1427816
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5,6,7,8-Tetrahydro-2-naphthol | HCID 14305 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 5-chloro-2,4-difluoro-N-(methylsulfonyl)benzamide | HCID 58042417 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 72545673 | HCID 72545673 | 30% |
| Product | HCID 86702842 | HCID 86702842 | 14% |
Reaction Steps
To a solution of 5,6,7,8-tetrahydronaphthalen-2-ol (66 mg, 0.44 mmol) in DMF (3 mL) was added NaH (19 mg, 0.48 mmol). After being stirred at room temperature for 0.5 h, 5-chloro-2,4-difluoro-N-(methylsulfonyl)benzamide (100 mg, 0.37 mmol) was added and the mixture was stirred at room temperature for 16 h. Sat. NH4Cl (10 mL) was added to quench the reaction and the resulting mixture was extracted with ethyl acetate (10 mL×3). The combined organic layer was dried over NaSO4 and concentrated in vacuo. The residue was purified by prep-HPLC (Gilson GX 281, Shim-pack PRC-ODS 250 mm×20 mm×2, gradient: CH3CN/10 mm/L NH4HCO3, 17 min) to afford 5-chloro-2-fluoro-N-(methylsulfonyl)-4-(5,6,7,8-tetrahydronaphthalen-2-yloxy)benzamide (44 mg, 30% yield) and 5-chloro-4-fluoro-N-(methylsulfonyl)-2-(5,6,7,8-tetrahydronaphthalen-2-yloxy)-benzamide (21 mg, 14% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08933236B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-0105205f98154cb88fae92c0ec7be40d |
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| Source note | uspto-grants-2015_01 |
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