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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274786Generated: October 31, 2026

tert-butyl 4-(6-fluoro-1-(phenylsulfonyl)-1H-indol-3-yl)-1H-pyrazole-1-carboxylate → tert-butyl 4-(1-(phenylsulfonyl)-6-(trifluoromethyl)-1H-indol-3-yl)-1H-pyrazole-1-carboxylate

https://huagongshe.com/reaction/2274786

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 4-(6-fluoro-1-(phenylsulfonyl)-1H-indol-3-yl)-1H-pyrazole-1-carboxylateHCID 118060266—
Reactant3-iodo-1-(phenylsulfonyl)-6-(trifluoromethyl)-1H-indoleHCID 118060607—
Producttert-butyl 4-(1-(phenylsulfonyl)-6-(trifluoromethyl)-1H-indol-3-yl)-1H-pyrazole-1-carboxylateHCID 118060358—

Reaction Steps

Following the general method as outlined in Intermediate 4, starting from 3-iodo-1-(phenylsulfonyl)-6-(trifluoromethyl)-1H-indole (Intermediate 40; 300 mg; 0.66 mmol) 0.40 g (94%) of the title compound was obtained as a black oil, which was used directly without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126984B2
Source datasetuspto-grants-2015_09
ORD IDord-e8735205e7234acaa3772215c9d711c1
Source noteuspto-grants-2015_09