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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005667Generated: October 31, 2026

Trifluoroacetic acid → HCID 9966428, compound

https://huagongshe.com/reaction/1005667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 60108779HCID 60108779—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 9966428HCID 9966428—

Reaction Steps

Trifluoroacetic acid (5 mL) was added to a solution of 4-(3-phenylsulfanyl-1H-indol-7-yl)piperazine-1-carboxylic acid tert-butyl ester (700 mg, 1.7 mmol), prepared as described in Example 1 Step 1, in 4 mL of dichloromethane. After 15 min the solution was diluted with water, basified with ammonium hydroxide, and extracted with dichloromethane. The dichloromethane was washed with brine and evaporated to afford 3-phenylsulfanyl-7-piperazin-1-yl-1H-indole (701) as a solid. The hydrochloride salt crystallized from ethanol-HCl to afford 500 mg of white solid, m.p. 300° C. Similarly replacing 4-(3-phenylsulfanyl-1H-indol-7-yl)piperazine-1-carboxylic acid tert-butyl ester with the appropriate sulfanyl derivatives, prepared as described in other examples herein, the following compounds were prepared:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787535B2
Source datasetuspto-grants-2004_09
ORD IDord-be4cc0024ff241b6abc2466bd0c5117e
Source noteuspto-grants-2004_09