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HRID 516707作成日:2026年10月25日

1,2-Dichloroethane → HCID 67467953、化合物

https://huagongshe.com/reaction/516707

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物4-MethylmorpholineHCID 7972—
反応物HOAtHCID 181649—
反応物3-(Aminomethyl)-6-methyl-4-propylpyridin-2(1H)-oneacetateHCID 67124140—
反応物1-(1-Methylethyl)-7-(methyloxy)-1H-indole-4-carboxylic acidHCID 67468682—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物HCID 67467953HCID 6746795360.8%

反応手順

Added 1-(1-methylethyl)-7-(methyloxy)-1H-indole-4-carboxylic acid (160 mg, 0.686 mmol), 3-(aminomethyl)-6-methyl-4-propyl-2(1H)-pyridinone (186 mg, 0.857 mmol), 1-hydroxy-7-azabenzotriazole (187 mg, 1.372 mmol), EDC (263 mg, 1.372 mmol) and N-methylmorpholine (0.302 mL, 2.74 mmol) to DMSO (10 mL) and stirred mixture at RT for 16 h. Added 25 ml of water and stirred for 10 minutes. Filtered off solids and dried in vacuo. The solids were purified by column chromatography (Biotage; 0% to 15% gradient MeOH:DCM; 10 g-HP-silica gel column) to give 165 mg of 1-(1-methylethyl)-N-[(6-methyl-2-oxo-4-propyl-1,2-dihydro-3-pyridinyl)methyl]-7-(methyloxy)-1H-indole-4-carboxamide. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.01 (t, 3H), 1.45 (d, J=6.57 Hz, 6H), 1.63 (m, J=7.45, 7.45, 7.45, 7.45, 7.33 Hz, 2H), 2.24 (s, 3H), 2.74 (t, J=7.58 Hz, 2H), 3.96 (s, 3H), 4.64 (br. s., 2H), 5.45 (quin, J=6.63 Hz, 1H), 5.97 (s, 1H), 6.62 (d, J=8.08 Hz, 1H), 6.94 (d, J=3.28 Hz, 1H), 7.24 (d, J=3.28 Hz, 1H), 7.53 (d, J=8.08 Hz, 1H), 7.74 (br. s., 1H), 12.46 (br. s., 1H). MS(ES) [M+H]+395.7.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09114141B2
出典データセットuspto-grants-2015_08
ORD IDord-a30a28414cf74236aff81bfb2f3f9ced
出典メモuspto-grants-2015_08