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N-bromobutanimide → 8-Bromo-6-pentyl-6,9-dihydro-5H-[1,2,4]triazolo[3,4-i]purin-5-one

HRID 2374306
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HRID 2374306 반응식
[CH2:1]([N:6]1[C:14]2[N:13]=[CH:12][NH:11][C:10]=2[C:9]2=[N:15][N:16]=[CH:17][N:8]2[C:7]1=[O:18])[CH2:2][CH2:3][CH2:4][CH3:5].[Br:19]N1C(=O)CCC1=O>C1COCC1>[Br:19][C:12]1[NH:11][C:10]2[C:9]3=[N:15][N:16]=[CH:17][N:8]3[C:7](=[O:18])[N:6]([CH2:1][CH2:2][CH2:3][CH2:4][CH3:5])[C:14]=2[N:13]=1
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참가 물질

4

반응물 2

HCID 67184N-bromobutanimideHCID 1359846986-Pentyl-6,9-dihydro-5H-[1,2,4]triazolo[3,4-i]purin-5-one

생성물 1

HCID 1359551378-Bromo-6-pentyl-6,9-dihydro-5H-[1,2,4]triazolo[3,4-i]purin-5-one수율 6.9%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
70 °C

실험 절차

To a mixture of 6-pentyl-6,9-dihydro-5H-[1,2,4]triazolo[3,4-i]purin-5-one (0.12 g, 0.487 mmol) in THF (5 mL) in a microwave reaction tube was added N-bromosuccinimide (0.20 g, 1.1 mmol). The mixture was heated at 70° C. in microwave oven for 12 min. After cooling down to room temperature, it was purified using preparative LCMS to provide the product (0.011 g). LCMS calculated for C11H14BrN6O (M+H): 325.0, 327.0; found: 325.0, 327.0.

후처리

  1. customin a microwave reaction tube
  2. temperatureAfter cooling down to room temperature
  3. customit was purified

출처 및 근거

ORD 기록
ord-c454cdf242d84c9681c1cd488f3d8f9b
출처 데이터셋
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07462624B2

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