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Tert-Butyl nitrite → 6-Bromo-5-fluorobenzo[d]thiazole

HRID 1890914
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HRID 1890914 반응식
[Br:1][C:2]1[C:11]([F:12])=[CH:10][C:5]2[N:6]=[C:7](N)[S:8][C:4]=2[CH:3]=1.C(ON=O)(C)(C)C>CN(C=O)C>[Br:1][C:2]1[C:11]([F:12])=[CH:10][C:5]2[N:6]=[CH:7][S:8][C:4]=2[CH:3]=1
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참가 물질

4

반응물 2

HCID 10906Tert-Butyl nitriteHCID 754809676-Bromo-5-fluoro-1,3-benzothiazol-2-amine

생성물 1

HCID 579109936-Bromo-5-fluorobenzo[d]thiazole수율 52%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
50 °C

실험 절차

To a solution of 6-bromo-5-fluoro-benzothiazol-2-ylamine (2.73 g, 11.05 mmol) in DMF (60 mL) was added tert-butylnitrite (1.58 mL, 13.26 mmol) dropwise. The reaction mixture was stirred at 50° C. for 3 h, then it was concentrated in vacuo. The residue was stirred in 1 N aqueous KOH for 10 min, then ethyl acetate was added and the mixture was stirred overnight. The insolubles were filtered, washed with water then ethyl acetate. The resulting filtrate was separated, and the organic layer was washed with brine and directly adsorbed on silica gel. Purification by flash chromatography on silica gel using a gradient of 0-30% ethyl acetate/hexane afforded 1.33 g of 6-bromo-5-fluoro-benzothiazole as a light yellow solid (52% yield): 1H NMR (DMSO-d6) δ 8.13 (d, 1H), 8.63 (d, 1H), 9.50 (s, 1H); MS (m/z) 232, 234 [M+H+]+.

후처리

  1. concentrationit was concentrated in vacuo
  2. stirringThe residue was stirred in 1 N aqueous KOH for 10 min
  3. additionethyl acetate was added
  4. stirringthe mixture was stirred overnight
  5. filtrationThe insolubles were filtered
  6. washwashed with water
  7. customThe resulting filtrate was separated
  8. washthe organic layer was washed with brine
  9. customPurification by flash chromatography on silica gel using a gradient of 0-30% ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-1fe29267e2644368ba49d1b60687d89b
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08507489B2

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