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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Bromine → 5-Bromo-1,3-benzothiazol-2-amine

HRID 2378559
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HRID 2378559 반응식
[Br:1][C:2]1[CH:3]=[C:4]([NH:8][C:9]([NH2:11])=[S:10])[CH:5]=[CH:6][CH:7]=1.BrBr>C(Cl)(Cl)Cl>[NH2:11][C:9]1[S:10][C:5]2[CH:6]=[CH:7][C:2]([Br:1])=[CH:3][C:4]=2[N:8]=1
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참가 물질

4

반응물 2

HCID 24408BromineHCID 2735619(3-Bromophenyl)thiourea

생성물 1

HCID 137757855-Bromo-1,3-benzothiazol-2-amine수율 47.6%

시약·촉매·용매 1

HCID 6212Chloroform용매2회

실험 절차

A solution of Intermediate 74 (1.29 g) in chloroform (12 ml) was added dropwise with a solution of bromine (272 μl, WAKO) in chloroform (1.5 ml), refluxed by heating for 2.5 hours, and stirred at room temperature for 16 hours. The reaction mixture was concentrated under reduced pressure, neutralized with 5% aqueous ammonia, and then added with water (50 ml) and methylene chloride (150 ml) for extraction. The organic layer was dried, and then the solvent was evaporated under reduced pressure. The residue was purified by column chromatography (Quad, hexane:ethyl acetate=2:1) to obtain the title compound (Intermediate 75, 609 mg).

후처리

  1. temperaturerefluxed
  2. temperatureby heating for 2.5 hours
  3. concentrationThe reaction mixture was concentrated under reduced pressure
  4. additionadded with water (50 ml) and methylene chloride (150 ml) for extraction
  5. customThe organic layer was dried
  6. customthe solvent was evaporated under reduced pressure
  7. customThe residue was purified by column chromatography (Quad, hexane:ethyl acetate=2:1)

출처 및 근거

ORD 기록
ord-80846b5db6684b528ad62e2bf20204d4
출처 데이터셋
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07470807B2

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