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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382027Generated: November 3, 2026

4-Methylmorpholine → HCID 59200019, compound

https://huagongshe.com/reaction/2382027

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
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—
ReactantHCID 68554956HCID 68554956—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 59200019HCID 5920001960%

Reaction Steps

4-Methyl-[2,2]bipyrimidinyl-5-carboxylic acid (0.5 g, 2.31 mmol) is combined with 5-fluoro-3-methyl-indol-1-yl-ammonium chloride (464 mg, 2.31 mmol), N-methylmorpholine (233 mg, 2.31 mmol) and DMF (10 mL). The suspension is stirred for 5 minutes at rt, then 4-(4,6-dimethoxy-[1,3,5]triazin-2-yl)-4-methyl-morpholin-4-ium chloride is added (640 mg, 2.31 mmol). The reaction is heated to 50° C. for 4 h. The reaction is then poured into water (50 mL), the suspension is chilled for 2 h in the refrigerator, and then filtered. The solids are then suspended in acetonitrile at 50° C. for 4 h, cooled, then filtered to afford 4-methyl-[2,2′]bipyrimidinyl-5-carboxylic acid (5-fluoro-3-methyl-indol-1-yl)-amide (60%). MS: 363 (M+H); 1H NMR (300 MHz, CDCl3): δ=2.27 (s, 3H), 2.77 (s, 3H), 7.07 (dt, 1H), 7.36 (dd, 1H), 7.38 (s, 1H), 7.44-7.48 (m, 1H), 7.70 (t, 1H), 9.05 (d, 2H), 9.29 (s, 1H), 11.9 (s, 1H). IC50=4.5 nM.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258130B2
Source datasetuspto-grants-2012_09
ORD IDord-4847beb681424c52b8e712c5103b6283
Source noteuspto-grants-2012_09