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Morpholine → 5-nitro-2-morpholino-3-(2H-1,2,3-triazol-2-yl)pyridine

HRID 1620101
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반응식

HRID 1620101 반응식
[NH:1]1[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.O1CCOCC1.Cl[C:14]1[C:19]([N:20]2[N:24]=[CH:23][CH:22]=[N:21]2)=[CH:18][C:17]([N+:25]([O-:27])=[O:26])=[CH:16][N:15]=1>O>[N+:25]([C:17]1[CH:18]=[C:19]([N:20]2[N:24]=[CH:23][CH:22]=[N:21]2)[C:14]([N:1]2[CH2:6][CH2:5][O:4][CH2:3][CH2:2]2)=[N:15][CH:16]=1)([O-:27])=[O:26]
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참가 물질

5

반응물 3

HCID 8083MorpholineHCID 312751,4-DioxaneHCID 866838702-chloro-5-nitro-3-(2H-1,2,3-triazol-2-yl)pyridine

생성물 1

HCID 866838765-nitro-2-morpholino-3-(2H-1,2,3-triazol-2-yl)pyridine

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Morpholine (0.5 ml) was added to a 1,4-dioxane solution (1 ml) containing 2-chloro-5-nitro-3-(2H-1,2,3-triazol-2-yl)pyridine (30 mg), followed by stirring at room temperature for 30 minutes. Water was added to the reaction solution, followed by extraction with ethyl acetate. The resultant was washed with saturated saline and dried over anhydrous sodium sulfate, the solvent was distilled away under reduced pressure, and a yellow solid of 5-nitro-2-morpholino-3-(2H-1,2,3-triazol-2-yl)pyridine (33 mg) was thus obtained.

후처리

  1. extractionfollowed by extraction with ethyl acetate
  2. washThe resultant was washed with saturated saline
  3. dry with materialdried over anhydrous sodium sulfate
  4. distillationthe solvent was distilled away under reduced pressure

출처 및 근거

ORD 기록
ord-623a7b8018ce4ea2ae9bf906f206543e
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08772320B2

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