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Ethyl isocyanate → 1-Ethyl-3-(6-methoxy-1,3-benzothiazol-2-yl)urea

HRID 712180
ノート
印刷プレビュー

反応式

HRID 712180 の反応式
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:6]2[N:7]=[C:8]([NH2:10])[S:9][C:5]=2[CH:4]=1.C(N(CC)CC)C.[CH2:20]([N:22]=[C:23]=[O:24])[CH3:21]>CS(C)=O>[CH2:20]([NH:22][C:23]([NH:10][C:8]1[S:9][C:5]2[CH:4]=[C:3]([O:2][CH3:1])[CH:12]=[CH:11][C:6]=2[N:7]=1)=[O:24])[CH3:21]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8022Ethyl isocyanateHCID 8471TriethylamineHCID 156302-Amino-6-methoxybenzothiazole

生成物 1

HCID 168004671-Ethyl-3-(6-methoxy-1,3-benzothiazol-2-yl)urea

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

実験手順

6-Methoxy-1,3-benzothiazol-2-amine (5.00 g, 27.74 mmol) was dissolved in anhydrous DMSO (20 mL) and triethylamine (15.50 mL, 110.97 mmol) followed by ethyl isocyanate (4.39 mL, 55.49 mmol). The mixture was stirred at rt under N2 for 4 h then quenched with water (˜200 mL) and stirred for 1 h. A white solid formed, was collected by filtration, rinsed with water then washed with acetone (100 mL) and the filtrate collected separately to the aqueous filtrate. The solid was partially soluble in acetone so the filtrate was concentrated to dryness under reduced pressure and combined with the solid collected by filtration to obtain the desired compound as a white solid, 6.27 g (90%). m/z: 251.96 [M+H]+.

後処理

  1. customthen quenched with water (˜200 mL)
  2. stirringstirred for 1 h
  3. customA white solid formed
  4. filtrationwas collected by filtration
  5. washrinsed with water
  6. washthen washed with acetone (100 mL)
  7. customthe filtrate collected separately to the aqueous filtrate
  8. concentrationwas concentrated to dryness under reduced pressure
  9. filtrationcollected by filtration

出典と根拠

ORDレコード
ord-307dcd8e1af84368808a594dc911e97a
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09181234B2

反応ノート

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