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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5,6,7,8-Tetrahydro-2-naphtholHCID 14305—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-chloro-2,4-difluoro-N-(methylsulfonyl)benzamideHCID 58042417—
SolventDimethylformamideHCID 6228—
ProductHCID 72545673HCID 7254567330%
ProductHCID 86702842HCID 8670284214%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933236B2
Source datasetuspto-grants-2015_01
ORD IDord-0105205f98154cb88fae92c0ec7be40d
Source noteuspto-grants-2015_01