Propanedioic acid, 2-amino-, 1,3-diethyl ester, hydrochloride (1:1) → methyl 3-amino-5-(tert-butyl)-1H-pyrrole-2-carboxylate

HRID 18925

반응식

HRID 18925 반응식
C[O-].[Na+].CC1C=CC(S(O[C:15]([C:19]([CH3:22])([CH3:21])[CH3:20])=[CH:16][C:17]#[N:18])(=O)=O)=CC=1.Cl.[NH2:24][CH:25](C(OCC)=O)[C:26]([O:28][CH2:29]C)=[O:27]>CO>[NH2:18][C:17]1[CH:16]=[C:15]([C:19]([CH3:20])([CH3:21])[CH3:22])[NH:24][C:25]=1[C:26]([O:28][CH3:29])=[O:27]

참가 물질

5

실험 절차

To a stirred sodium methoxide solution (15% by weight, 80 mL total) was added drop-wise a solution of 1-cyano-3,3-dimethylbut-1-en-2-yl 4-methylbenzenesulfonate (10.0 g, 36 mmol) and diethyl aminomalonate hydrochloride salt (9.0 g, 43 mmol) in methanol (50 mL). After the addition was completed, the reaction was stirred at room temperature for 2 hours, the solvent was removed under vacuum and the crude product was dissolved in water and extracted with ethyl acetate. The combined organic layers was washed with brine, dried and the solvent removed under vacuum. The crude product was purified by column chromatography (silicagel, dichloromethane:methanol 95:5) to afford 2.4 g of the desired methyl 3-amino-5-tert-butyl-1H-pyrrole-2-carboxylate used as such in the next step.

후처리

  1. additionAfter the addition
  2. customthe solvent was removed under vacuum
  3. dissolutionthe crude product was dissolved in water
  4. extractionextracted with ethyl acetate
  5. washThe combined organic layers was washed with brine
  6. customdried
  7. customthe solvent removed under vacuum
  8. customThe crude product was purified by column chromatography (silicagel, dichloromethane:methanol 95:5)

출처 및 근거

ORD 기록
ord-dbed93c467224da4b16a268bb97437de
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07741479B2

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