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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561710Generated: October 26, 2026

(4-Chloro-2-methylphenyl)(4-fluorophenyl)methanol → 3-[(4-Chloro-2-methylphenyl)(4-fluorophenyl)methyl]-5-fluoro-7-[(methylsulfanyl)methyl]-1H-indole

https://huagongshe.com/reaction/561710

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Chloro-2-methylphenyl)(4-fluorophenyl)methanolHCID 58392095—
Reactant3-[Bis(4-fluorophenyl)methyl]-7-[(methylsulfanyl)methyl]-1H-indoleHCID 58392127—
Reactant5-Fluoro-7-[(methylsulfanyl)methyl]-1H-indoleHCID 58392227—
Product3-[(4-Chloro-2-methylphenyl)(4-fluorophenyl)methyl]-5-fluoro-7-[(methylsulfanyl)methyl]-1H-indoleHCID 58392221—

Reaction Conditions

Temperature80 °C

Reaction Steps

The title compound was prepared starting from 500 mg (2.56 mmol) of the compound from Example 11A and 706 mg (2.56 mmol) of the compound from Example 83A in analogy to the synthesis of the compound from Example 278. A difference was that stirring at 80° C. was for only 4 h. 616 mg (56% of theory) of the target compound were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063234B2
Source datasetuspto-grants-2011_11
ORD IDord-80838b15ecb2421eb1318190daec9277
Source noteuspto-grants-2011_11