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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Formamide → HCID 178497210, 화합물

HRID 930189
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인쇄 미리보기

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HRID 930189 반응식
[NH2:1][C:2]1[NH:3][C:4]2[C:9]([C:10]=1[C:11](OCC)=[O:12])=[CH:8][CH:7]=[C:6]([C:16]([O:18][CH3:19])=[O:17])[CH:5]=2.C([O-])=O.[NH4+].[CH:24]([NH2:26])=O>O>[OH:12][C:11]1[C:10]2[C:9]3[C:4](=[CH:5][C:6]([C:16]([O:18][CH3:19])=[O:17])=[CH:7][CH:8]=3)[NH:3][C:2]=2[N:1]=[CH:24][N:26]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 713FormamideHCID 2723923Ammonium formateHCID 59447961HCID 59447961, 화합물

생성물 1

HCID 178497210HCID 178497210, 화합물수율 107.9%

시약·촉매·용매 1

HCID 962Water용매

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온도
165 °C

실험 절차

In a 100 mL round-bottom flask were added 3-ethyl 6-methyl 2-amino-1H-indole-3,6-dicarboxylate (1.1 g, 4.19 mmol), ammonium formate (0.53 g, 8.39 mmol), and formamide (16.7 mL, 419 mmol) to give a tan suspension which was heated to 165° C. for 12 hours. The mixture was allowed to cool to room temperature and water was added. The resulting precipitate was filtered, air-dried and dried under high vacuum overnight to afford 1.1 g of the title compound. LCMS m/z 244.2 (M+H)+, retention time (on analytical HPLC)=1.51 minutes.

후처리

  1. customto give a tan suspension which
  2. temperatureto cool to room temperature
  3. filtrationThe resulting precipitate was filtered
  4. customair-dried
  5. customdried under high vacuum overnight

출처 및 근거

ORD 기록
ord-cedcbe7939b8407ca75aae2f9a7ed1f4
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09296744B2

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