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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43024Generated: October 25, 2026

Triethylamine → N-(5-((4-(hydroxymethyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)methyl)-2,3-dihydro-1H-inden-1-yl)-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-sulfonamide

https://huagongshe.com/reaction/43024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Methyl-3-(trifluoromethyl)-1H-pyrazole-4-sulfonyl chlorideHCID 2794561—
Reactant(1-((1-Amino-2,3-dihydro-1H-inden-5-yl)methyl)-3-(trifluoromethyl)-1H-pyrazol-4-yl)methanolHCID 58230802—
SolventDichloromethaneHCID 6344—
ProductN-(5-((4-(hydroxymethyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)methyl)-2,3-dihydro-1H-inden-1-yl)-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-sulfonamideHCID 53326549—

Reaction Steps

To a solution of (1-((1-amino-2,3-dihydro-1H-inden-5-yl)methyl)-3-(trifluoromethyl)-1H-pyrazol-4-yl)methanol (0.096 mmol, 30 mg) and triethylamine (0.193 mmol, 0.027 mL, 19.50 mg) in DCM (0.9 mL) was added 1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-sulfonyl chloride (0.096 mmol, 23.96 mg) and the whole stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure and the residue purified by RP-HPLC to give a clear film (12.0 mg, 0.023 mmol, 23.8%). MS (ESI): m/z [M+H]+ 524.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536214B2
Source datasetuspto-grants-2013_09
ORD IDord-f77c6ad3e18f4285bce73753e2dec1e1
Source noteuspto-grants-2013_09