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HRID 626906作成日:2026年10月27日

Hydrochloric Acid → Methyl 4-methyl-6-[4-(trifluoromethyl)phenyl]pyrimidine-2-carboxylate

https://huagongshe.com/reaction/626906

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物WaterHCID 962—
反応物p-tolylmethyl N-(pyrazine-2-carbonylamino)carbamateHCID 478568—
反応物4-Methyl-6-[4-(trifluoromethyl)phenyl]pyrimidine-2-carbonitrileHCID 57468709—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
溶媒Sodium CarbonateHCID 10340—
生成物Methyl 4-methyl-6-[4-(trifluoromethyl)phenyl]pyrimidine-2-carboxylateHCID 9001507694%

反応条件

温度80 °C

反応手順

Concentrated aq. hydrochloric acid (42 mL, 491.4 mmol) was added to a stirred suspension of 4-methyl-6-[4-(trifluoromethyl)phenyl]pyrimidine-2-carbonitrile [CAS: 951232-17-0] (8.3 g, 31.53 mmol) in methanol (248 mL). The stirred mixture was heated at block temperature of 80° C. for 20 h. The reaction mixture was cooled to ambient temperature, diluted with DCM (500 ml) and Na2CO3 solid was added with stirring. Water (500 ml) was added and the mixture transferred to a separating funnel and shaken (aqueous phase had pH10). The aq. phase was re-extracted with DCM (200 ml) and the combined organic layers were dried (Na2SO4) and evaporated to an oil which solidified, to give 7.6 g after drying. This was dissolved in DCM (30 ml) and the solution was applied to a 340 g silica cartridge which was then eluted on a Biotage SP4 system with a gradient of EtOAc/iso-hexane from 0-75% to give methyl 4-methyl-6-[4-(trifluoromethyl)phenyl]pyrimidine-2-carboxylate (D29) (6.1 g, approximately 94% pure, contaminated with decarboxylated material);

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09309254B2
出典データセットuspto-grants-2016_04
ORD IDord-5af05b864aa940ceaa4065926d01a251
出典メモuspto-grants-2016_04