Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043769Generated: October 29, 2026

Triethylamine → N-(2,3-dihydro-2-methyl-1H-inden-1-yl)-N-methyl-2-[1-[[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl]-4-piperidinyl]-4-thiazolecarboxamide

https://huagongshe.com/reaction/2043769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,3-dihydro-N,2-dimethyl-1H-inden-1-amineHCID 61751197—
Reactant2-[1-[[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl]-4-piperidinyl]-4-thiazolecarbonyl chlorideHCID 86637727—
SolventDichloromethaneHCID 6344—
ProductN-(2,3-dihydro-2-methyl-1H-inden-1-yl)-N-methyl-2-[1-[[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl]-4-piperidinyl]-4-thiazolecarboxamideHCID 6679591339.4%

Reaction Steps

To a solution of 2,3-dihydro-N,2-dimethyl-1H-inden-1-amine (177 mg, 1.1 mmol) and triethylamine (0.22 mL, 1.6 mmol) in 5 mL of dichloromethane was gradually added 2-[1-[[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl]-4-piperidinyl]-4-thiazolecarbonyl chloride (421 mg, 1 mmol) (i.e. the product of Example 19, Step D) at 0° C. The reaction mixture was stirred at room temperature for 16 h, diluted with 4 mL of dichloromethane, and washed with water, 1 N aqueous hydrochloric acid, water, saturated solution of sodium bicarbonate and brine. The filtered reaction mixture was dried over magnesium sulfate and concentrated in vacuo to give 215 mg of the title compound, the product of present invention as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586611B2
Source datasetuspto-grants-2013_11
ORD IDord-32a8ddc848924e2c974cde9b2bb7f505
Source noteuspto-grants-2013_11