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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382066Generated: November 3, 2026

4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride → 2-(3-Fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid (6-trifluoromethyl-indol-1-yl)-amide

https://huagongshe.com/reaction/2382066

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chlorideHCID 2734059—
Reactant2-(3-Fluorophenyl)-4-methylpyrimidine-5-carboxylic acidHCID 61702587—
Reactant1H-Indol-1-amine, 6-(trifluoromethyl)-HCID 68553185—
SolventDimethylformamideHCID 6228—
SolventSodium CarbonateHCID 10340—
Product2-(3-Fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid (6-trifluoromethyl-indol-1-yl)-amideHCID 5919996644%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid (278 mg, 1.2 mmol) and 6-trifluoromethyl-indol-1-ylamine (200 mg, 1 mmol) in DMF (5 mL) is stirred at 50° C. for 0.5 h. The mixture is treated with DMTMM (290 mg, 1.05 mmol) and stirred at 50° C. for 1 h. The mixture is diluted with saturated aqueous Na2CO3 (5 mL) and extracted with EtOAc (3×50 mL). The combined organic layer is dried (Na2SO4), filtered and concentrated in vacuo. The residue is triturated with Et2O/heptane overnight. The precipitate is collected by filtration, washed with H2O (50 mL) and heptane (50 mL), and dried in vacuo to afford 2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid (6-trifluoromethyl-indol-1-yl)-amide (180 mg, 44%). MS: 415 (M+H); 1H NMR (300 MHz, DMSO-d6): δ 12.09 (s, NH, 1H), 9.33 (s, 1H), 8.35 (d, 1H), 8.20 (d, 1H), 7.90 (s, 1H), 7.79 (m, 2H), 7.65 (m, 1H), 7.46 (m, 2H), 6.74 (d, 1H), 2.79 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258130B2
Source datasetuspto-grants-2012_09
ORD IDord-b344cfdb46bd4a1ebee7ab7a05774484
Source noteuspto-grants-2012_09