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

HRID 2058853
ノート
印刷プレビュー

反応式

HRID 2058853 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

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

生成物 1

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

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-e525fcfbc1654ba9a1aa81e43617d687
出典データセット
uspto-grants-1982_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04319914

反応ノート

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