Diisopropylethylamine → 2-methoxy-2-methyl-N-(5-phenylethynyl-pyridin-2-yl)-propionamide

HRID 40542ノート

反応式

HRID 40542 の反応式
[C:1]1([C:7]#[C:8][C:9]2[CH:10]=[CH:11][C:12]([NH2:15])=[N:13][CH:14]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:16][O:17][C:18]([CH3:23])([CH3:22])[C:19](O)=[O:20].F[B-](F)(F)F.BrC1C=CC=C[N+]=1CC.CCN(C(C)C)C(C)C>ClCCl>[CH3:16][O:17][C:18]([CH3:23])([CH3:22])[C:19]([NH:15][C:12]1[CH:11]=[CH:10][C:9]([C:8]#[C:7][C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)=[CH:14][N:13]=1)=[O:20]

参加物

6

反応物 4

HCID 81531DiisopropylethylamineHCID 27363002-Bromo-1-ethylpyridinium tetrafluoroborateHCID 98554652-Methoxy-2-methylpropanoic acidHCID 468541905-Phenylethynyl-pyridin-2-ylamine

生成物 1

HCID 715483422-methoxy-2-methyl-N-(5-phenylethynyl-pyridin-2-yl)-propionamide収率 46.2%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

(100 mg, 0.515 mmol) 5-Phenylethynyl-pyridin-2-ylamine (Example 1, step 1) was dissolved in dichloromethane (5 ml) and 2-methoxy-2-methylpropionic acid (91 mg, 0.77 mmol, 1.5 equiv.), 2-bromo-1-ethyl pyridinium tetrafluoroborate (CAS 878-23-9) (211 mg, 0.77 mmol, 1.5 equiv.) and Hunig's Base (0.26 ml, 1.54 mmol, 3 equiv.) were added. The mixture was stirred for 14 hours at room temperature. The reaction mixture was extracted with saturated Na2CO3 solution and dichloromethane. The organic layer was dried over sodium sulfate and evaporated to dryness. The crude product was purified by prep HPLC to afford the desired 2-methoxy-2-methyl-N-(5-phenylethynyl-pyridin-2-yl)-propionamide (70 mg, 46% yield) was obtained as a yellow oil, MS: m/e=295.2 (M+H+).

後処理

  1. extractionThe reaction mixture was extracted with saturated Na2CO3 solution and dichloromethane
  2. dry with materialThe organic layer was dried over sodium sulfate
  3. customevaporated to dryness
  4. customThe crude product was purified by prep HPLC

出典と根拠

ORDレコード
ord-98a07b23b5e94b878356f0ee97fa61bd
出典データセット
uspto-grants-2013_09
特許番号
US08530472B2

反応ノート

読み込み中…