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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275354Generated: November 1, 2026

HCID 10471407, compound → HCID 10381888, compound

https://huagongshe.com/reaction/275354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10471407HCID 10471407—
CatalystAdams' catalystHCID 345198—
SolventAcetic AcidHCID 176—
ProductHCID 10381888HCID 1038188881.8%

Reaction Steps

6-Chloro-3-(4-fluorophenyl)-1-(4-pyridyl)-lH-indole 2e (1.8 g) was dissolved in acetic acid (100 ml) and PtO2 (0.2 g) was added. After hydrogenation for 30 h at 3 ato the catalyst was filtered off, the acetic acid was evaporated in vacuo and water (50 ml) was added. The acidic solution was made alkaline (pH>9) with concentrated sodium hydroxide and extracted with ethyl acetate (2×50 ml). The combined organic phases were successively washed with diluted sodium hydroxide (50 ml), washed with brine, and dried (Na2SO4). Evaporation of the solvent gave 1.5 g of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05393761
Source datasetuspto-grants-1995_02
ORD IDord-a7eae7849ca74017907dd78b268f0587
Source noteuspto-grants-1995_02