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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269942Generated: November 1, 2026

Sodium Hydroxide → HCID 178431630, compound

https://huagongshe.com/reaction/1269942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium MethoxideHCID 10942334—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 178473989HCID 178473989—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178431630HCID 17843163064%

Reaction Steps

Under a nitrogen atmosphere, 28%-sodium methoxide (64 μl, 0.311 mmol) was added at 0° C. to a suspension of cis-1-{4-[(1-acetyl-4-methyl-1H-indazol-5-yl)oxy]cyclohexyl}pyrrolidine-2,5-dione (500 mg, 0.311 mmol) in a mixture of methanol (3 ml) and tetrahydrofuran (3 ml). After 10 minutes, a saturated aqueous ammonium chloride solution was added to the reaction solution and the resulting mixture was poured into water and extracted with ethyl acetate. The extract solution was concentrated under reduced pressure, and to a solution of the resulting residue in tetrahydrofuran (4 ml) was added lithium aluminum hydride (47 mg, 1.25 mmol) and the resulting mixture was refluxed. After 4 hours, water, a 2M-aqueous sodium hydroxide solution and water were added thereto in that order, and the resulting mixture was filtered by the use of Celite. The filtrate was concentrated under reduced pressure and the resulting residue was purified by a silica gel column chromatography (eluent: chloroform/methanol→chloroform/methanol (1%-aqueous ammonia)) to obtain cis-4-methyl-5-[(4-pyrrolidin-1-ylcyclohexyl)oxy]-1H-indazole (59.6 mg, 64%) and cis-4({4-methyl-1H-indazol-5-yl}oxy)cyclohexyl}amino)butan-1-ol (15.4 mg, 16%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199147B2
Source datasetuspto-grants-2007_04
ORD IDord-0670548a7c054c4786497a5f9f60f18c
Source noteuspto-grants-2007_04