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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382068Generated: November 2, 2026

4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride → 4-Methyl-[2,2']bipyrimidinyl-5-carboxylic acid (6-trifluoromethyl-indol-1-yl)-amide

https://huagongshe.com/reaction/2382068

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chlorideHCID 2734059—
Reactant4-Methyl-2-(pyrimidin-2-yl)pyrimidine-5-carboxylic acidHCID 61699985—
Reactant1H-Indol-1-amine, 6-(trifluoromethyl)-HCID 68553185—
SolventDimethylformamideHCID 6228—
SolventSodium CarbonateHCID 10340—
Product4-Methyl-[2,2']bipyrimidinyl-5-carboxylic acid (6-trifluoromethyl-indol-1-yl)-amideHCID 5919994625.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 4-methyl-[2,2′]bipyrimidinyl-5-carboxylic acid (259 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 4-methyl-[2,2′]bipyrimidinyl-5-carboxylic acid (6-trifluoromethyl-indol-1-yl)-amide (100 mg, 25%). MS: 399 (M+H); 1H NMR (300 MHz, DMSO-d6): δ 12.16 (s, NH, 1H), 9.39 (s, 1H), 9.06 (d, 2H), 7.92 (s, 1H), 7.81 (m, 2H), 7.70 (t, 1H), 7.44 (d, 1H), 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-1580fd5aa718431297d82ec796f8a272
Source noteuspto-grants-2012_09