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Benzoyl isothiocyanate → 1-Benzoyl-3-(4-methoxy-7-phenyl-benzothiazol-2-yl)-thiourea

HRID 1060287
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HRID 1060287 반응식
[NH2:1][C:2]1[S:3][C:4]2[C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)=[CH:9][CH:8]=[C:7]([O:17][CH3:18])[C:5]=2[N:6]=1.[C:19]([N:27]=[C:28]=[S:29])(=[O:26])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>O1CCOCC1>[C:19]([NH:27][C:28]([NH:1][C:2]1[S:3][C:4]2[C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)=[CH:9][CH:8]=[C:7]([O:17][CH3:18])[C:5]=2[N:6]=1)=[S:29])(=[O:26])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 68284Benzoyl isothiocyanateHCID 222830262-Amino-4-methoxy-7-phenyl-benzothiazole

생성물 1

HCID 222831071-Benzoyl-3-(4-methoxy-7-phenyl-benzothiazol-2-yl)-thiourea수율 55%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

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온도
100 °C

실험 절차

To a suspension of 2-amino-4-methoxy-7-phenyl-benzothiazole (1.52 g, 6 mmol) in dioxane (60 ml) was added benzoylisothiocyanate (1.45 g, 8.9 mmol) and the mixture heated to 100° C. for 2 h, during which time the suspension dissolved. After cooling the solvent was removed and the solids suspended in hot acetonitrile (100 ml) and filtered while warm (50° C.). The solid collected was washed with acetonitrile (20 ml) then dried under vacuum (0.05 mmHg), at 60° C. to afford the title compound as a pale yellow amorphous solid (1.38 g, 55% yield), MS: m/e=419.0 (M+).

후처리

  1. dissolutiondissolved
  2. temperatureAfter cooling the solvent
  3. customwas removed
  4. filtrationfiltered
  5. temperaturewhile warm (50° C.)
  6. customThe solid collected
  7. washwas washed with acetonitrile (20 ml)
  8. customthen dried under vacuum (0.05 mmHg), at 60° C.

출처 및 근거

ORD 기록
ord-4cfa91df2f2b4d25bea589f0c96db8f8
출처 데이터셋
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06521754B2

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