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Ammonia → N,N-diallyl-4-aminopyridine-3-sulfonamide

HRID 2283345
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HRID 2283345 반응식
[CH2:1]([N:4]([CH2:15][CH:16]=[CH2:17])[S:5]([C:8]1[CH:9]=[N:10][CH:11]=[CH:12][C:13]=1Cl)(=[O:7])=[O:6])[CH:2]=[CH2:3].[I-].[Li+].[NH3:20]>>[CH2:1]([N:4]([CH2:15][CH:16]=[CH2:17])[S:5]([C:8]1[CH:9]=[N:10][CH:11]=[CH:12][C:13]=1[NH2:20])(=[O:7])=[O:6])[CH:2]=[CH2:3]
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참가 물질

4

반응물 3

HCID 222AmmoniaHCID 66321Lithium iodideHCID 57750928N,N-diallyl-4-chloropyridine-3-sulfonamide

생성물 1

HCID 57750998N,N-diallyl-4-aminopyridine-3-sulfonamide수율 59%

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온도
120 °C

실험 절차

A mixture of N,N-diallyl-4-chloropyridine-3-sulfonamide (1.5 g, 5.5 mmol), lithium iodide (0.74 g, 5.5 mmol) and ammonia (7 M in methanol, 14 mL, 5.5 mmol) under an atmosphere of argon was heated at 120° C. for 2 h in a microwave reactor. Silica was added and the solvent was evaporated. Purification by column chromatography, using chloroform/methanol (95:5) as the eluent, gave the title compound in 59% yield.

후처리

  1. additionSilica was added
  2. customthe solvent was evaporated
  3. customPurification by column chromatography

출처 및 근거

ORD 기록
ord-e073639fe2e344d79c611e80ecf47c27
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09145380B2

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