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HRID 1046845作成日:2026年10月26日

Pyridine → N-{(7R)-6-Cyano-7-(4-cyanophenyl)-5-methyl-4-[3-(trifluoromethyl)phenyl]-4,7-dihydro[1,2,4]-triazolo[1,5-a]pyrimidin-2-yl}-1-fluorocyclopropanecarboxamide

https://huagongshe.com/reaction/1046845

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物1-Fluorocyclopropanecarbonyl chlorideHCID 54101822—
反応物(7R)-2-amino-7-(4-cyanophenyl)-5-methyl-4-[3-(trifluoromethyl)phenyl]-4,7-dihydro[1,2,4]triazolo[1,5-a]pyrimidine-6-carbonitrile hydrochlorideHCID 66627899—
溶媒TetrahydrofuranHCID 8028—
生成物N-{(7R)-6-Cyano-7-(4-cyanophenyl)-5-methyl-4-[3-(trifluoromethyl)phenyl]-4,7-dihydro[1,2,4]-triazolo[1,5-a]pyrimidin-2-yl}-1-fluorocyclopropanecarboxamideHCID 66627850—

反応手順

Under an atmosphere of argon protective gas, (7R)-2-amino-7-(4-cyanophenyl)-5-methyl-4-[3-(trifluoromethyl)phenyl]-4,7-dihydro[1,2,4]triazolo[1,5-a]pyrimidine-6-carbonitrile hydrochloride (30 mg, 66 μmol) was dissolved in abs. pyridine (1.5 ml). At room temperature, 1-fluorocyclopropanecarbonyl chloride (20 mg, 165 μmol, 2.5 eq.) in abs. THF (1 ml) was added in two portions, and the mixture was stirred for 12 h. The reaction mixture was then concentrated under reduced pressure and directly purified by preparative HPLC (Kromasil C18 column, 5 μm, 50×20 mm; mobile phase: acetonitrile-water-0.1% TFA). After lyophilization, the product was obtained as a solid (29.5 mg, 89% of theory).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08569314B2
出典データセットuspto-grants-2013_10
ORD IDord-13aa1084487a43bea84124d3c0fa2649
出典メモuspto-grants-2013_10