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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 57781097, 화합물 → HCID 57781140, 화합물

HRID 1690718
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HRID 1690718 반응식
[CH:1]([C:3]1[N:7]([CH:8]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[C:11](=[O:18])[O:10][C:9]2([CH3:20])[CH3:19])[CH:6]=[N:5][CH:4]=1)=[CH2:2]>CO.[Pd]>[CH2:1]([C:3]1[N:7]([CH:8]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[C:11](=[O:18])[O:10][C:9]2([CH3:19])[CH3:20])[CH:6]=[N:5][CH:4]=1)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 57781097HCID 57781097, 화합물

생성물 1

HCID 57781140HCID 57781140, 화합물

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To a solution of 4-(5-vinyl-imidazol-1-yl)-3,3-dimethyl-isochroman-1-one (0.049 g, 0.173 mmol) (Example 3) in methanol (1 mL) is added Pd/C (10% wt, 0.009 g, 0.009 mmol) and the flask is flushed with hydrogen. The mixture is stirred under balloon pressure. After 3 h, another portion of catalyst (0.009 g) is added. After 7 h, the mixture is filtered and concentrated in vacuo to give 4-(5-ethyl-imidazol-1-yl)-3,3-dimethyl-isochroman-1-one as a white solid; MS (ESI) m/z 271.2 (M+H); 1H NMR (400 MHz, MeOD) δ ppm 1.25 (s, 3 H), 1.43 (br. s., 3 H), 1.56 (s, 3 H), 2.87 (br. s, 2 H), 5.55 (br. s, 1 H), 6.83 (s, 1 H), 7.17 (br. s, 1 H), 7.45 (d, J=7.6 Hz, 1 H), 7.67 (td, J=7.6, 1.0 Hz, 1 H), 7.78 (td, J=7.6, 1.3 Hz, 1 H), 8.24 (dd, J=7.6, 1.0 Hz, 1 H).

후처리

  1. custom0.009 g, 0.009 mmol) and the flask is flushed with hydrogen
  2. additionanother portion of catalyst (0.009 g) is added
  3. waitAfter 7 h
  4. filtrationthe mixture is filtered
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-414e5db2bf4c4410aee91d7eb7a4c6db
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08153674B2

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