Nitrogen → HCID 86690320、化合物

HRID 1428670ノート

反応式

HRID 1428670 の反応式
Br[C:2]1[C:3]([NH2:22])=[N:4][C:5]([C:15]2[CH:20]=[CH:19][C:18]([CH3:21])=[CH:17][CH:16]=2)=[C:6]([C:8]2[CH:13]=[CH:12][C:11]([CH3:14])=[CH:10][CH:9]=2)[N:7]=1.N#N.C(N(CC)CC)C.[C:32]([OH:40])(=[O:39])[CH2:33][CH2:34][CH2:35][CH2:36][C:37]#[CH:38]>O1CCOCC1.C(Cl)Cl.[Cu]I.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].C(Cl)Cl>[NH2:22][C:3]1[C:2]([C:38]#[C:37][CH2:36][CH2:35][CH2:34][CH2:33][C:32]([OH:40])=[O:39])=[N:7][C:6]([C:8]2[CH:13]=[CH:12][C:11]([CH3:14])=[CH:10][CH:9]=2)=[C:5]([C:15]2[CH:20]=[CH:19][C:18]([CH3:21])=[CH:17][CH:16]=2)[N:4]=1

参加物

9

実験手順

3-Bromo-5,6-di-p-tolylpyrazin-2-amine (Example 1, step 3) (200 mg, 0.565 mmol) in anhydrous dioxane (10 ml), degassed with N2 was treated with triethylamine (0.708 ml, 5.08 mmol), hept-6-ynoic acid (0.179 ml, 1.129 mmol), copper(I) iodide (32.3 mg, 0.169 mmol) and PdCl2(dppf)-CH2Cl2-adduct (46.1 mg, 0.056 mmol). The reaction mixture was stirred at room temperature for 16 hours. The resulting mixture was diluted with DCM (10 ml) and dry loaded onto silica. Purification by chromatography on silica eluting with 0-100% EtOAc in iso-hexane followed by 20% MeOH in EtOAc afforded the titled compound;

後処理

  1. customdry
  2. customPurification by chromatography on silica eluting with 0-100% EtOAc in iso-hexane

出典と根拠

ORDレコード
ord-07da27e6c5d74023a883e081e6320407
出典データセット
uspto-grants-2015_01
特許番号
US08937069B2

反応ノート

読み込み中…