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Sodium Azide → 2-[6-(Azidomethyl)-2-pyridyl]propan-2-ol

HRID 2207554
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HRID 2207554 반응식
Br[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([C:9]([OH:12])([CH3:11])[CH3:10])[N:4]=1.[N-:13]=[N+:14]=[N-:15].[Na+]>CN(C)C=O>[N:13]([CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([C:9]([OH:12])([CH3:11])[CH3:10])[N:4]=1)=[N+:14]=[N-:15]
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참가 물질

4

반응물 2

HCID 33557Sodium AzideHCID 667183882-(6-(Bromomethyl)pyridin-2-yl)propan-2-ol

생성물 1

HCID 866553202-[6-(Azidomethyl)-2-pyridyl]propan-2-ol

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

2-Bromomethyl-6-(1-hydroxy-1-methylethyl)pyridine (7.61 g, 33 mmol) was dissolved in dimethylformamide (100 mL) and sodium azide (2.6 g, 39.7 mmol) added. After stirring the resultant mixture overnight at ambient temperature, the reaction was poured into dicholoromethane and washed well with water. The organic layer was dried (magnesium sulphate), filtered and concentrated to dryness. The resulting yellow oil (5.88 g, 93%) was used without further purification; NMR δH (400 MHz, CDCl3) 7.70 (1H, t, J 7.8 Hz), 7.30 (1H, d, J 8.0 Hz), 7.19 (1H, d, J 7.8 Hz), 4.82 (1H, br s), 4.42 (2H, s), 1.51 (6H, s); LC-MS Retention time 2.06 min, (M+H)+ 193.

후처리

  1. additionthe reaction was poured into dicholoromethane
  2. washwashed well with water
  3. dry with materialThe organic layer was dried (magnesium sulphate)
  4. filtrationfiltered
  5. concentrationconcentrated to dryness
  6. customThe resulting yellow oil (5.88 g, 93%) was used without further purification

출처 및 근거

ORD 기록
ord-4eaeba2a21994c7fa09142d05a398ae3
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09376443B2

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