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Chemical Structure| 1224096-01-8 Chemical Structure| 1224096-01-8

Structure of 1224096-01-8

Chemical Structure| 1224096-01-8

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Product Details of [ 1224096-01-8 ]

CAS No. :1224096-01-8
Formula : C16H22F3N3O3
M.W : 361.36
SMILES Code : O=C(N1C[C@H](OC2=C(N)C=C(C(F)(F)F)C=C2N)CC1)OC(C)(C)C
MDL No. :MFCD28142651

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* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1224096-01-8 ]

[ 1224096-01-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 16490-02-1 ]
  • [ 1224096-01-8 ]
  • [ 1224096-02-9 ]
YieldReaction ConditionsOperation in experiment
79.1% With 4-methyl-morpholine; 2-chloro-4,6-dimethoxy-1 ,3,5-triazine; In tetrahydrofuran; at 20℃; for 24.5h;Product distribution / selectivity; 2-Chloro-4,6-dimethoxy-1,3,5-triazine (5.97 g, 34 mmol) was stirred in anhydrous THF (200 mL). N-Methylmorpholine (7.5 ml, 68 mmol) was added. The resulting mixture was stirred at room temperature for 30 minutes. Then, (R)-tert-butyl 3-(2,6-diamino-4-(trifluoromethyl)phenoxy)pyrrolidine-1-carboxylate (10.84 g, 30 mmol) and <strong>[16490-02-1]pyrimidine-4,6-dicarboxylic acid</strong> (2.48 g, 14.8 mmol) were added. The mixture was stirred at room temperature for 24 hours. The solvent was evaporated completely in vacuum. Water (250 mL) was added and the mixture was stirred for 4 hours. After filtration, the yellow cake was washed with water (3×100 mL) and stirred in water (250 mL) for 4 hours. The filtration and washing procedure was repeated twice. The solid was dried in the air and stirred in dichloromethane (20 mL) for 30 minutes, followed by ultrasonic treatment for 1 hour. After filtration, the yellow cake was quickly washed with cold dichloromethane (2×10 mL). The product (10.0 g, yield: 79.1%) was used as such for subsequent reaction
With pyridine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; at 20℃; for 25h;Inert atmosphere; Large scale; Compound 4 (1.6 kg) is coupled with <strong>[16490-02-1]pyrimidine-4,6-dicarboxylic acid</strong> (383 g) in the presence of 1-[(3-(dimethylamino)-propyl)]-3-ethylcarbodiirnide hydrochloride (1.29 kg), in pyridine, under inert atmosphere, at ambient temperature. After 25 hours, the reaction mixture is diluted in water (92 kg), a solid is separated out, which is collected by filtration and dried at 37-40C, and crude compound is purified by trituration with ethyl acetate/heptanes for three times. Yield: 1.34 kg (70%), expected Purity about: 87.5%.
 

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