戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1623352作成日:2026年10月25日

(2R)-2-(trifluoromethyl)oxirane → HCID 178521649、化合物

https://huagongshe.com/reaction/1623352

反応式

関与物質

役割名称HCID仕込み量
反応物(2R)-2-(trifluoromethyl)oxiraneHCID 7016923—
反応物HCID 178511591HCID 178511591—
溶媒IsopropanolHCID 3776—
生成物HCID 178521649HCID 17852164999.4%

反応条件

温度60 °C

反応手順

To a solution of N2′-(trans-4-aminocyclohexyl)-5′-chloro-N6-((tetrahydro-2H-pyran-4-yl)methyl)-2,4′-bipyridine-2′,6-diamine (50 mg, 0.120 mmol) in 2-propanol (0.8 mL) was added (R)-(+)-3,3,3-trifluoro-1,2-epoxypropane (10.4 uL, 0.120 mmol). The mixture was stirred at 60° C. for 17 hr. The reaction mixture was concentrated. The resulting residue was purified by reverse phase HPLC and lyophilized to give 63 mg of (R)-3-(trans-4-(5′-chloro-6-((tetrahydro-2H-pyran-4-yl)methyl)amino-2,4′-bipyridin-2′-yl-amino)cyclohexylamino)-1,1,1-trifluoropropan-2-ol as its TFA salt. LCMS (m/z): 528.3 (MH+), retention time=0.53 min; 1H NMR (400 MHz, DMSO-d6) δ ppm 1.08-1.34 (m, 4H) 1.36-1.56 (m, 2H) 1.61 (d, J=12.52 Hz, 2H) 1.70-1.90 (m, 1H) 2.04 (d, J=9.39 Hz, 3H) 2.13 (d, J=11.74 Hz, 1H) 2.97-3.19 (m, 4H) 3.24 (t, J=10.76 Hz, 3H) 3.64 (d, J=10.96 Hz, 1H) 3.83 (dd, J=10.96, 2.74 Hz, 2H) 4.36-4.50 (m, 2H) 6.54-6.68 (m, 2H) 6.70 (d, J=7.04 Hz, 0H) 6.94 (br. s., 0H) 7.23 (br. s., 0H) 7.53 (br. s., 0H) 8.04 (s, 0H) 8.76 (br. s., 2H)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08778951B2
出典データセットuspto-grants-2014_07
ORD IDord-63adb7c45efd45978690c5d68f0faaed
出典メモuspto-grants-2014_07