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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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3,4-Difluorobenzaldehyde → HCID 178526788, 화합물

HRID 506600
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HRID 506600 반응식
[NH2:1][C:2]1[C:7]([NH2:8])=[CH:6][C:5]([N+:9]([O-:11])=[O:10])=[CH:4][N:3]=1.[F:12][C:13]1[CH:14]=[C:15]([CH:18]=[CH:19][C:20]=1[F:21])[CH:16]=O>[N+](C1C=CC=CC=1)([O-])=O>[F:12][C:13]1[CH:14]=[C:15]([C:16]2[NH:1][C:2]3=[N:3][CH:4]=[C:5]([N+:9]([O-:11])=[O:10])[CH:6]=[C:7]3[N:8]=2)[CH:18]=[CH:19][C:20]=1[F:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 5880883,4-DifluorobenzaldehydeHCID 34801515-Nitropyridine-2,3-diamine

생성물 1

HCID 178526788HCID 178526788, 화합물수율 27.9%

시약·촉매·용매 1

HCID 7416Nitrobenzene용매

실험 절차

1.00 g 2,3-diamino-5-nitro-pyridine and 0.95 g 3,4-difluorobenzaldehyde were stirred in 60 ml nitrobenzene at 160° C. for 26 hrs. The solvent was removed under vacuum and the residue dissolved in 40 ml pyridine at 60° C. The solution was cooled in an ice bath. Precipitated product was isolated by filtration and dried to yield 0.5 g of the title product.

후처리

  1. customThe solvent was removed under vacuum
  2. dissolutionthe residue dissolved in 40 ml pyridine at 60° C
  3. temperatureThe solution was cooled in an ice bath
  4. customPrecipitated product was isolated by filtration
  5. customdried

출처 및 근거

ORD 기록
ord-99788fbfa8dd4e889b5ae55cc64a8b39
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07786113B2

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