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Potassium cyanate → 2-(Diaminomethyleneamino)-4-(2-ureidomethylthiazol-4-yl)thiazole

HRID 2379841
ノート
印刷プレビュー

反応式

HRID 2379841 の反応式
[NH2:1][CH2:2][C:3]1[S:4][CH:5]=[C:6]([C:8]2[N:9]=[C:10]([N:13]=[C:14]([NH2:16])[NH2:15])[S:11][CH:12]=2)[N:7]=1.[O-:17][C:18]#[N:19].[K+]>O>[NH2:15][C:14](=[N:13][C:10]1[S:11][CH:12]=[C:8]([C:6]2[N:7]=[C:3]([CH2:2][NH:1][C:18]([NH2:19])=[O:17])[S:4][CH:5]=2)[N:9]=1)[NH2:16]
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 2

HCID 11378442Potassium cyanateHCID 189538084-(2-Aminomethylthiazol-4-yl)-2-(diaminomethyleneamino)thiazole

生成物 1

HCID 189537912-(Diaminomethyleneamino)-4-(2-ureidomethylthiazol-4-yl)thiazole収率 29.9%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A solution of 4-(2-aminomethylthiazol-4-yl)-2-(diaminomethyleneamino)thiazole (1.0 g) and potassium cyanate (0.5 g) in water (50 ml) was stirred for 3.5 hours at room temperature. The resulting precipitate was collected by filtration. The precipitate was suspended in water (30 ml) and then a saturated aqueous potassium carbonate solution (20 ml) was added. The mixture was stirred for 1 hour at room temperature. The resulting precipitate was collected by filtration. Recrystallization from a mixture of methanol and water afforded 2-(diaminomethyleneamino)-4-(2-ureidomethylthiazol-4-yl)thiazole (0.35 g).

後処理

  1. filtrationThe resulting precipitate was collected by filtration
  2. additiona saturated aqueous potassium carbonate solution (20 ml) was added
  3. filtrationThe resulting precipitate was collected by filtration
  4. customRecrystallization
  5. additionfrom a mixture of methanol and water

出典と根拠

ORDレコード
ord-5992a17c3b444dd585617984e13c4602
出典データセット
uspto-grants-1994_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05364871

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート