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

HRID 40542노트

반응식

HRID 40542 반응식
[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]

참가 물질

6

반응물 4

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

생성물 1

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

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

(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+).

후처리

  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

출처 및 근거

ORD 기록
ord-98a07b23b5e94b878356f0ee97fa61bd
출처 데이터셋
uspto-grants-2013_09
특허 번호
US08530472B2

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