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Triethylamine → 2-(4-Bromo-2-fluorobenzyl)-1,3-dioxo-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-4-carboxylic acid (-)-menthyl ester

HRID 256589
노트
인쇄 미리보기

반응식

HRID 256589 반응식
[CH:1]1([CH3:30])[CH2:6][CH2:5][CH:4]([CH:7]([CH3:9])[CH3:8])[CH:3]([O:10][C:11](=[O:29])[CH:12]([N:18]2[CH:22]=[CH:21][CH:20]=[C:19]2[C:23](=[O:28])C(Cl)(Cl)Cl)[C:13](OCC)=[O:14])[CH2:2]1.Cl.[Br:32][C:33]1[CH:40]=[CH:39][C:36]([CH2:37][NH2:38])=[C:35]([F:41])[CH:34]=1.C(N(CC)CC)C>CN(C)C=O>[CH:1]1([CH3:30])[CH2:6][CH2:5][CH:4]([CH:7]([CH3:8])[CH3:9])[CH:3]([O:10][C:11]([CH:12]2[N:18]3[CH:22]=[CH:21][CH:20]=[C:19]3[C:23](=[O:28])[N:38]([CH2:37][C:36]3[CH:39]=[CH:40][C:33]([Br:32])=[CH:34][C:35]=3[F:41])[C:13]2=[O:14])=[O:29])[CH2:2]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 184681974-Bromo-2-fluorobenzylamine hydrochlorideHCID 536822462-(2-Trichloroacetylpyrrol-1-yl)malonic acid ethyl (-)-menthyl ester

생성물 1

HCID 867473472-(4-Bromo-2-fluorobenzyl)-1,3-dioxo-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-4-carboxylic acid (-)-menthyl ester수율 78.7%

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매

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온도
75 °C

실험 절차

A mixture of 2-(2-trichloroacetylpyrrol-1-yl)malonic acid ethyl (-)-menthyl ester (87.0 g), 4-bromo-2-fluorobenzylamine hydrochloride (53.0 g) and triethylamine (66.4 g, 91.0 ml) in anhydrous dimethylformamide (200 ml) was stirred under the stream of nitrogen at 75° C. for 2 hours. The reaction mixture was concentrated under reduced pressure and the residue was dissolved in ethyl acetate. The solution was washed with 5% cold hydrochloric acid and then with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, and evaporated under reduced pressure. The residue was recrystallized from methanol to give the title compound (74.0 g, 78.7%) as colorless crystals, mp 98°-99° C.

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. dissolutionthe residue was dissolved in ethyl acetate
  3. washThe solution was washed with 5% cold hydrochloric acid
  4. dry with materialwith saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate
  5. customevaporated under reduced pressure
  6. customThe residue was recrystallized from methanol

출처 및 근거

ORD 기록
ord-efe1eeb916da40f484cf2a3149a501c1
출처 데이터셋
uspto-grants-1993_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05258382

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