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Nitric Acid → 2,4-Diamino-5-(7-methoxy-8-nitro-5-quinolylmethyl)pyrimidine

HRID 280026
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HRID 280026 반응식
[NH2:1][C:2]1[N:7]=[C:6]([NH2:8])[C:5]([CH2:9][C:10]2[CH:19]=[C:18]([O:20][CH3:21])[CH:17]=[C:16]3[C:11]=2[CH:12]=[CH:13][CH:14]=[N:15]3)=[CH:4][N:3]=1.[N+:22]([O-])([OH:24])=[O:23].[OH-].[Na+]>S(=O)(=O)(O)O>[NH2:1][C:2]1[N:7]=[C:6]([NH2:8])[C:5]([CH2:9][C:10]2[CH:19]=[C:18]([O:20][CH3:21])[C:17]([N+:22]([O-:24])=[O:23])=[C:16]3[C:11]=2[CH:12]=[CH:13][CH:14]=[N:15]3)=[CH:4][N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 944Nitric AcidHCID 14798Sodium HydroxideHCID 128497902,4-Diamino-5-(7-methoxy-5-quinolylmethyl)pyrimidine

생성물 1

HCID 128497932,4-Diamino-5-(7-methoxy-8-nitro-5-quinolylmethyl)pyrimidine

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

To a cold (5°) solution of 2,4-diamino-5-(7-methoxy-5-quinolylmethyl)pyrimidine (0.28 g, 1.0 mmol) in concentrated sulfuric acid (2 mL) was added dropwise 90% nitric acid (0.10 g, 1.4 mmol). After stirring at 5° for 30 min, the reation was poured onto ice and the resulting solution taken to pH 3 with 5N sodium hydroxide. The tan solid that separated was collected then boiled in water and filtered to remove insolubles. The filtrate was taken to pH 8 with 1M sodium carbonate to precipitate the title compound (0.14 g, 42%); mp >270° dec. Anal. Calcd for C15H14N6O3 : C, 55.21; H, 4.32; N, 25.75. Found: C, 55.02, H, 4.10; N, 25.41.

후처리

  1. additionthe reation was poured onto ice
  2. customThe tan solid that separated was collected
  3. filtrationfiltered
  4. customto remove insolubles
  5. customto precipitate the title compound (0.14 g, 42%)

출처 및 근거

ORD 기록
ord-8273d94d34ac4bc29cd2117b753ceb6f
출처 데이터셋
uspto-grants-1986_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04587342

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