Sodium Hydroxide → 5-Hydrazinyl-2-(methylsulfonyl)pyridine

HRID 1815108노트

반응식

HRID 1815108 반응식
[NH2:1][C:2]1[CH:3]=[N:4][C:5]([S:8]([CH3:11])(=[O:10])=[O:9])=[CH:6][CH:7]=1.[N:12]([O-])=O.[Na+].O.O.[Sn](Cl)Cl.[OH-].[Na+]>Cl.O.O1CCCC1>[NH:1]([C:2]1[CH:7]=[CH:6][C:5]([S:8]([CH3:11])(=[O:10])=[O:9])=[N:4][CH:3]=1)[NH2:12]

참가 물질

8

실험 절차

To a solution of 3-amino-6-(methylsulfonyl)pyridine (3.72 g, 21.6 mmol) in concentrated hydrochloric acid (30 mL), sodium nitrite (1.78 g, 25.7 mmol) in water (20 mL) was added dropwise at −10° C. to −15° C. and the mixture was stirred for 2 hours at −10° C. to −5° C. (Note: the reaction was monitored by thin layer chromatography to make sure all the starting material was consumed). Tin(II) chloride dihydrate (20 g, 88.6 mmol) in concentrated hydrochloric acid (30 mL) was added dropwise at −5° C. The mixture was stirred 1 hour at −5° C. and then left overnight. The mixture was basified with aqueous sodium hydroxide (pH=9) with ice cooling and tetrahydrofuran (200 mL) was added and stirred for 30 minutes. The mixture was filtered by Celite® and the filtrate was extracted with tetrahydrofuran (200 mL×3). The organic extraction was combined and dried over magnesium sulfate and concentrated under reduced pressure to provide the title compound (3.2 g, 78.8%).

후처리

  1. customwas consumed)
  2. stirringThe mixture was stirred 1 hour at −5° C.
  3. waitleft overnight
  4. additionwas added
  5. stirringstirred for 30 minutes
  6. filtrationThe mixture was filtered by Celite®
  7. extractionthe filtrate was extracted with tetrahydrofuran (200 mL×3)
  8. extractionThe organic extraction
  9. dry with materialdried over magnesium sulfate
  10. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-16410dcb420a4cf7b682cbea8415b7d2
출처 데이터셋
uspto-grants-2005_04
특허 번호
US06878726B2

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