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Hydroxyamine hydrochloride → HCID 67328311, 화합물

HRID 1846145
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HRID 1846145 반응식
CC1[N:3]([C:8]2[N:13]=[C:12]([CH3:14])[C:11]([O:15][CH2:16][C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[C:10]([CH3:23])[N:9]=2)C(C)=CC=1.Cl.NO>C(O)C.O.O>[NH2:3][C:8]1[N:13]=[C:12]([CH3:14])[C:11]([O:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[C:10]([CH3:23])[N:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 443297Hydroxyamine hydrochlorideHCID 67353995HCID 67353995, 화합물

생성물 1

HCID 67328311HCID 67328311, 화합물

시약·촉매·용매 2

HCID 962Water용매HCID 19096565Water ethanol용매

실험 절차

To a stirred solution containing 2.85 g (9.27 mmol) 2-(2,5-dimethyl-1H-pyrrol-1-yl)-5-benzyloxy-4,6-dimethylpyrimidine (6) in 30 mL of ethanol-water 1:1 were added 6.44 g (93 mmol) of hydroxylamine hydrochloride. The reaction mixture was stirred at reflux overnight under argon atmosphere. The pH of the solution was then brought to 10 and diluted with 20 mL of water. The mixture was extracted with two portions of 30 mL of dichloromethane. The combined organic solution was dried (MgSO4) and then concentrate under diminished pressure. The residue was purified by chromatography on a silica gel column. Elution with acetone-hexanes 1:2 gave the expected product as white solid. Yield: 2.1 g (98%). 1H-NMR (CDCl3) δ 7.39 (m, 5H), 4.80 (br. 2H), 4.74 (s, 2H), 2.29 (s, 6H). 13C-NMR (CDCl3) 160.05, 158.45, 141.50, 137.02, 37.27, 19.22.

후처리

  1. temperatureat reflux overnight under argon atmosphere
  2. extractionThe mixture was extracted with two portions of 30 mL of dichloromethane
  3. dry with materialThe combined organic solution was dried (MgSO4)
  4. concentrationconcentrate under diminished pressure
  5. customThe residue was purified by chromatography on a silica gel column
  6. washElution with acetone-hexanes 1:2

출처 및 근거

ORD 기록
ord-1088901b215c42c5ba60b05a09161f9a
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08952025B2

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