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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Aniline → HCID 59468599, 화합물

HRID 1012188
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HRID 1012188 반응식
[Cl:1][C:2]1[N:7]=[C:6]([C:8]2[S:12][C:11]([CH:13]=O)=[CH:10][CH:9]=2)[CH:5]=[CH:4][N:3]=1.[NH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>CC(O)=O.CC(N(C)C)=O>[Cl:1][C:2]1[N:7]=[C:6]([C:8]2[S:12][C:11]([CH2:13][NH:15][C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)=[CH:10][CH:9]=2)[CH:5]=[CH:4][N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6115AnilineHCID 59857089HCID 59857089, 화합물

생성물 1

HCID 59468599HCID 59468599, 화합물수율 59.4%

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 31374Dimethylacetamide용매

실험 절차

[5-(2-Chloro-pyrimidin-4-yl)-thiophene-2-carbaldehyde (100 mg, 0.446 mmol) was dissolved in 25% HOAc in DMA (4 mL) and was treated with aniline (61 uL, 0.669 mmol) for 2 h. MP-CNBH3 resin was added the reaction was shaken for 18 h. The reaction was filtered and rinsed with DMA and the solution was concentrated in vacuo. The crude material was purified by SiO2 chromatography using a gradient 0-100% hexanes/EtOAc to afford title compound (80 mg, 59%).

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후처리

  1. additionMP-CNBH3 resin was added the reaction
  2. filtrationThe reaction was filtered
  3. washrinsed with DMA
  4. concentrationthe solution was concentrated in vacuo
  5. customThe crude material was purified by SiO2 chromatography

출처 및 근거

ORD 기록
ord-809eacd92de6437c9e7cb24e2d89399b
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07977481B2

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