2,6-Diamino-3-nitropyridine → 3-Phenylpyrido[2,3-b]pyrazin-6-ylamine

HRID 2252717

반응식

HRID 2252717 반응식
[NH2:1][C:2]1[C:7]([N+:8]([O-])=O)=[CH:6][CH:5]=[C:4]([NH2:11])[N:3]=1.O.[C:13]1([C:19]([CH:21]=O)=O)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>C(O)C.[Ni]>[C:13]1([C:19]2[N:1]=[C:2]3[N:3]=[C:4]([NH2:11])[CH:5]=[CH:6][C:7]3=[N:8][CH:21]=2)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

참가 물질

5

반응물 2

HCID 3199982,6-Diamino-3-nitropyridineHCID 12215922Glyoxal, phenyl-, hydrate

생성물 1

HCID 121331983-Phenylpyrido[2,3-b]pyrazin-6-ylamine

시약·촉매·용매 2

HCID 935Nickel촉매HCID 702Ethanol용매2회

실험 절차

A solution of 1.22 g of 2,6-diamino-3-nitropyridine (7.92 mmol) in 210 ml of ethanol is hydrogenated with Raney nickel as catalyst at 50° C. and 5 bar. After the hydrogenation is complete, the catalyst is filtered off with suction through a glass fibre filter. Before the filtration, 1.68 g of phenylglyoxal hydrate (11.03 mmol) are introduced into 50 ml of ethanol in the receiver. The catalyst is then filtered off under nitrogen as protective gas, and the hydrogenation solution is sucked directly into the reaction flask. The greenish blue reaction mixture is heated under reflux under nitrogen for 30 min. The mixture is allowed to cool, and the solvent is removed in vacuo. A dark brown solid is finally obtained. Purification by column chromatography on silica gel (mobile phase dichloromethane/methanol mixture) affords a pale yellow crystalline solid.

후처리

  1. filtrationthe catalyst is filtered off with suction through a glass fibre filter
  2. filtrationThe catalyst is then filtered off under nitrogen as protective gas
  3. customThe greenish blue reaction mixture
  4. temperatureis heated
  5. temperatureunder reflux under nitrogen for 30 min
  6. temperatureto cool
  7. customthe solvent is removed in vacuo
  8. customA dark brown solid is finally obtained
  9. customPurification by column chromatography on silica gel (mobile phase dichloromethane/methanol mixture)
  10. customaffords a pale yellow crystalline solid

출처 및 근거

ORD 기록
ord-2f14b7456e33449ba9a820e9d585bafb
출처 데이터셋
uspto-grants-2008_01
특허 번호
US07323468B2

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