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Formaldehyde → HCID 68629339, 화합물

HRID 1182718
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HRID 1182718 반응식
[Br:1][C:2]1[N:11]2[C:5]([CH2:6][NH:7][CH2:8][C:9]3[CH:15]=[C:14]([Cl:16])[CH:13]=[CH:12][C:10]=32)=[N:4][N:3]=1.C=O.[C:19]([BH3-])#N.[Na+]>CO>[Br:1][C:2]1[N:11]2[C:5]([CH2:6][N:7]([CH3:19])[CH2:8][C:9]3[CH:15]=[C:14]([Cl:16])[CH:13]=[CH:12][C:10]=32)=[N:4][N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 712FormaldehydeHCID 5003444Sodium cyanoborohydrideHCID 67363168HCID 67363168, 화합물

생성물 1

HCID 68629339HCID 68629339, 화합물수율 30.4%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A mixture of 1-bromo-8-chloro-5,6-dihydro-4H-2,3,5,10b-tetraaza-benzo[e]azulene (1.9 g, 6.4 mmol) and paraformaldehyde (1.5 g, 51 mmol) in methanol (64 ml) was heated at reflux for 16 h. After cooling to 0° C. sodium cyanoborohydride (0.8 g, 13 mmol) was added. The reaction mixture was allowed to warm to room temperature and stirred for 3 h. After quenching with 1 M aqueous sodium hydroxide solution (200 ml) the aqueous layer was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo. Flash chromatography over aminopropyl-modified silica gel with n-heptane/ethyl acetate as eluent gave the title compound (0.61 g) as white solid with a purity of ca. 85% as assessed by 1H-NMR. MS m/e: 313 (M+H+).

후처리

  1. temperaturewas heated
  2. temperatureat reflux for 16 h
  3. additionwas added
  4. customAfter quenching with 1 M aqueous sodium hydroxide solution (200 ml) the aqueous layer
  5. extractionwas extracted with ethyl acetate
  6. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-f7bd9bd0a989408992d8c0ec69ad584e
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08664216B2

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