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N-bromobutanimide → 7-Bromo-2-methyl-4-benzoxazolamine

HRID 1441824
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HRID 1441824 반응식
[NH2:1][C:2]1[C:7]2[N:8]=[C:9]([CH3:11])[O:10][C:6]=2[CH:5]=[CH:4][CH:3]=1.[Br:12]N1C(=O)CCC1=O>CN(C=O)C>[NH2:1][C:2]1[C:7]2[N:8]=[C:9]([CH3:11])[O:10][C:6]=2[C:5]([Br:12])=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 67184N-bromobutanimideHCID 106068972-Methyl-1,3-benzoxazol-4-amine

생성물 1

HCID 218751637-Bromo-2-methyl-4-benzoxazolamine수율 56.3%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
-5 °C

실험 절차

Compound 474B (3.90 g, 26.3 mmol) was dissolved in DMF (45 mL) and cooled to −5° C. and N-bromosuccinimide (4.68 g, 26.3 mmol) was added in small portions and the reaction stirred for 5 h. The mixture was poured into 150 mL of ice water to give a cream colored solid which was filtered, washed with water, dissolved in CH2Cl2, dried over MgSO4, filtered and concentrated in vacuo. Purification of the crude material by flash chromatography on silica gel eluting with 20% ether/CH2Cl2 gave compound 474C (3.36 g, 56%) as a beige solid. HPLC: 95.4% at 2.583 min (retention time) (YMC S5 ODS column, 4.6×50 mm, eluting with 10-90% aqueous methanol over 4 min containing 0.2% phosphoric acid, 4 mL/min, monitoring at 220 nm). MS (ES): f/z 228.03 [M+H]+.

후처리

  1. customto give a cream colored solid which
  2. filtrationwas filtered
  3. washwashed with water
  4. dissolutiondissolved in CH2Cl2
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customPurification of the crude material by flash chromatography on silica gel eluting with 20% ether/CH2Cl2

출처 및 근거

ORD 기록
ord-f797055febf34bf08da7358fa6f55217
출처 데이터셋
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07655689B2

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