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Benzoyl isothiocyanate → 3-(Benzoylcarbamothioylamino)-5-methoxy-benzoic acid

HRID 712277
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인쇄 미리보기

반응식

HRID 712277 반응식
[C:1]([N:9]=[C:10]=[S:11])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:12][C:13]1[CH:14]=[C:15]([CH:19]=[C:20]([O:22][CH3:23])[CH:21]=1)[C:16]([OH:18])=[O:17]>CC(C)=O>[C:1]([NH:9][C:10]([NH:12][C:13]1[CH:14]=[C:15]([CH:19]=[C:20]([O:22][CH3:23])[CH:21]=1)[C:16]([OH:18])=[O:17])=[S:11])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 68284Benzoyl isothiocyanateHCID 138744093-Amino-5-methoxybenzoic acid

생성물 1

HCID 866639903-(Benzoylcarbamothioylamino)-5-methoxy-benzoic acid

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

Benzoyl isothiocyanate (169 μl, 1.25 mmol) was added to a solution of 3-amino-5-methoxy-benzoic acid (0.2 g, 1.19 mmol) in acetone (10 mL). The reaction was stirred at ambient temperature and a thick precipitate formed after 10 minutes. LCMS indicated complete conversion of the starting material. The solvent was removed in vacuo and the crude material triturated with iso-hexane, dried under reduced pressure and used directly in the next step.

후처리

  1. customa thick precipitate formed after 10 minutes
  2. customThe solvent was removed in vacuo
  3. customthe crude material triturated with iso-hexane
  4. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-574c1603f968414688ff491d6571f2b4
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09181234B2

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