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Toluene → 2-[1-Methyl-3-(5,5,7-trimethyl-4,5,6,7-tetrahydrobenzothiazol-2-yl)ureido]acetaldehyde

HRID 2058853
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인쇄 미리보기

반응식

HRID 2058853 반응식
[CH3:1][C:2]1([CH3:15])[CH2:13][C:6]2[N:7]=[C:8]([N:10]=[C:11]=[O:12])[S:9][C:5]=2[CH:4]([CH3:14])[CH2:3]1.C[CH:17]([NH2:20])[CH:18]=[O:19].[C:21]1(C)C=CC=CC=1>>[CH3:21][N:20]([CH2:17][CH:18]=[O:19])[C:11]([NH:10][C:8]1[S:9][C:5]2[CH:4]([CH3:14])[CH2:3][C:2]([CH3:15])([CH3:1])[CH2:13][C:6]=2[N:7]=1)=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 1140TolueneHCID 188982AlaninalHCID 539537435,5,7-Trimethyl-4,5,6,7-tetrahydrobenzothiazol-2-yl isocyanate

생성물 1

HCID 205484682-[1-Methyl-3-(5,5,7-trimethyl-4,5,6,7-tetrahydrobenzothiazol-2-yl)ureido]acetaldehyde

실험 절차

5,5,7-Trimethyl-4,5,6,7-tetrahydrobenzothiazol-2-yl isocyanate dimer (7.5 grams), the dimethyl acetal of 2-methyl-aminoacetaldehyde (5 grams) and toluene (15 ml) were charged into a glass reaction vessel equipped with a mechanical stirrer and reflux condenser. The reaction mixture was then heated, with stirring for a period of about 1 hour. After this time the mixture was cooled and filtered. The filtrate was washed with water, dried and evaporated, leaving the desired product dimethyl acetal of 2-[1-methyl-3-(5,5,7-trimethyl-4,5,6,7-tetrahydrobenzothiazol-2-yl)ureido]acetaldehyde as a brown oil.

후처리

  1. customequipped with a mechanical stirrer
  2. temperaturereflux condenser
  3. temperatureThe reaction mixture was then heated
  4. temperatureAfter this time the mixture was cooled
  5. filtrationfiltered
  6. washThe filtrate was washed with water
  7. customdried
  8. customevaporated

출처 및 근거

ORD 기록
ord-e525fcfbc1654ba9a1aa81e43617d687
출처 데이터셋
uspto-grants-1982_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04319914

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