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Sodium Chloride → 3-Amino-2-imino-6-methyl-2,3-dihydropyrimidin-4(1H)-one

HRID 591221
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HRID 591221 반응식
CC[O-].[Na+].[Na].[C:6]([NH:9][NH2:10])([NH2:8])=[NH:7].Cl.[Na+].[Cl-].O=[C:15]([CH3:22])[CH2:16][C:17](OCC)=[O:18]>C(O)C>[NH2:7][C:6]1[N:9]([NH2:10])[C:17](=[O:18])[CH:16]=[C:15]([CH3:22])[N:8]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 5234Sodium ChlorideHCID 8868Ethyl AcetoacetateHCID 2723922Sodium ethoxideHCID 5360545SodiumHCID 178418668HCID 178418668, 화합물

생성물 1

HCID 9131753-Amino-2-imino-6-methyl-2,3-dihydropyrimidin-4(1H)-one

시약·촉매·용매 1

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
HCID 702
Ethanol
용매

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온도
50 °C

실험 절차

To a stirring solution of NaOEt prepared from sodium (FLUKA, 9.19 g, 400 mmol) and ethanol (350 mL) was added aminoguanidine hydrochloride (ALDRICH, 44.2 g, 400 mmol). The reaction mixture was heated at 50° C. for 30 min. Then, the mixture was filtered to remove NaCl, and ethyl 3-oxobutanoate (ALDRICH, 25.3 mL, 200 mmol) was added to the filtrate. The reaction mixture was heated under reflux for 5 h and, then, stirred at room temperature overnight. The precipitate obtained was filtered and dried under vacuum to afford Intermediate 1 as a pale pink solid.

후처리

  1. filtrationThen, the mixture was filtered
  2. additionwas added to the filtrate
  3. temperatureThe reaction mixture was heated
  4. temperatureunder reflux for 5 h
  5. customThe precipitate obtained
  6. filtrationwas filtered
  7. customdried under vacuum

출처 및 근거

ORD 기록
ord-14cd1255a38d4f75999a61648930ba35
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09238653B2

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