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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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5-Methyl-1,2-oxazole-3-carbaldehyde → 1-{[(5-Methyl-1,2-oxazol-3-yl)methylidene]amino}imidazolidin-2-one

HRID 25928
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인쇄 미리보기

반응식

HRID 25928 반응식
[CH3:1][C:2]1[O:6][N:5]=[C:4]([CH:7]=O)[CH:3]=1.Cl.[NH2:10][N:11]1[CH2:15][CH2:14][NH:13][C:12]1=[O:16]>O>[CH3:1][C:2]1[O:6][N:5]=[C:4]([CH:7]=[N:10][N:11]2[CH2:15][CH2:14][NH:13][C:12]2=[O:16])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 27952225-Methyl-1,2-oxazole-3-carbaldehydeHCID 192616781-Amino-2-imidazolidinone hydrochloride

생성물 1

HCID 542211301-{[(5-Methyl-1,2-oxazol-3-yl)methylidene]amino}imidazolidin-2-one

시약·촉매·용매 1

HCID 962Water용매

실험 절차

14.0 pts. by wt. of 5-methyl-3-formyl-isoxazole are reacted with 25.6 pts. by wt. of 1-amino-2-oxo-imidazolidine hydrochloride in 100 pts. by vol. of water as in Example 25.1. After 90 minutes, the precipitate is filtered off, washed with water, dried and recrystallised from absolute acetonitrile. 12.5 pts. by wt. of 1-(5-methyl-isoxazol-3-yl-methyleneamino)-2-oxo-imidazolidine of melting point 195°-7° C. are obtained.

후처리

  1. filtrationthe precipitate is filtered off
  2. washwashed with water
  3. customdried
  4. customrecrystallised from absolute acetonitrile

출처 및 근거

ORD 기록
ord-139d17def34245298714a3e2a6ba331f
출처 데이터셋
uspto-grants-1979_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04147693

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