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Hydrochloric Acid → N-(5-bromopyridin-3-yl)benzenesulfonamide

HRID 1695753
ノート
印刷プレビュー

反応式

HRID 1695753 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([NH2:8])[CH:5]=[N:6][CH:7]=1.[C:9]1([S:15](Cl)(=[O:17])=[O:16])[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.Cl>N1C=CC=CC=1>[Br:1][C:2]1[CH:3]=[C:4]([NH:8][S:15]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)(=[O:17])=[O:16])[CH:5]=[N:6][CH:7]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 313Hydrochloric AcidHCID 7369Benzenesulfonyl chloride2 回HCID 8176813-Amino-5-bromopyridine

生成物 1

HCID 57843412N-(5-bromopyridin-3-yl)benzenesulfonamide

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

反応条件

温度
0 °C

実験手順

5-Bromo-3-pyridinamine (5 g) was dissolved in pyridine (150 ml) and the reaction was cooled to 0° C. in an ice-bath and stirred for 5 min. Benzenesulfonyl chloride (1.86 ml) was added dropwise and the reaction was stirred at 0° C. for 3 hr. Further benzenesulfonyl chloride (1.86 ml) was added and the reaction continued stirring for 1 hr. The reaction was neutralised with 2 M HCl and extracted with DCM (60 ml) then evaporated to dryness. The residue was dissolved in DCM and preadsorbed on fluorosil then purified by column chromatography on silica, eluting with 1-5% MeOH/DCM, to give the title compound (8 g).

後処理

  1. stirringthe reaction was stirred at 0° C. for 3 hr
  2. stirringthe reaction continued stirring for 1 hr
  3. extractionextracted with DCM (60 ml)
  4. customthen evaporated to dryness
  5. dissolutionThe residue was dissolved in DCM
  6. customthen purified by column chromatography on silica
  7. washeluting with 1-5% MeOH/DCM

出典と根拠

ORDレコード
ord-70354769617245258533d00922bef3e1
出典データセット
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08163743B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート