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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18175Generated: October 27, 2026

Water → HCID 68588019, compound

https://huagongshe.com/reaction/18175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethyl SulfideHCID 1068—
ReactantHCID 68585750HCID 68585750—
ReactantHCID 178511841HCID 178511841—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68588019HCID 68588019—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 3-benzyl-7-(4-tert-butoxycarbonyl-piperazin-1-yl)-indole-1-carboxylic acid tert-butyl ester (186 mg, 0.38 mmol) in THF (5 ml) was cooled to −78° C., and Sec-BuLi (1.4 ml, 1.4 M in cyclohexane) was added. After stirring at −78° C. for 20 minutes, 1 ml of dimethyl sulfide was added and the reaction was allowed to warm up to room temperature for 30 minutes. H2O was slowly added, followed by EtOAC. The organic layer was separated and washed with water and brine. After drying over MgSO4, the organic fraction was concentrated in vacuo to give crude 3-benzyl-7-(4-tert-butoxycarbonyl-piperazin-1-yl)-2-methylsulfanyl-indole-1-carboxylic acid tert-butyl ester as an oil (277 mg), which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741326B2
Source datasetuspto-grants-2010_06
ORD IDord-412b0496ce594ecfa72406626de76218
Source noteuspto-grants-2010_06