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

HRID 712180
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HRID 712180 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

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

생성물 1

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

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

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]+.

후처리

  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

출처 및 근거

ORD 기록
ord-307dcd8e1af84368808a594dc911e97a
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09181234B2

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