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Isopropylamine → HCID 10632459、化合物

HRID 2210419
ノート
印刷プレビュー

反応式

HRID 2210419 の反応式
Cl[C:2]1[CH:7]=[CH:6][N:5]=[CH:4][C:3]=1[S:8]([NH2:11])(=[O:10])=[O:9].[CH:12]([NH2:15])([CH3:14])[CH3:13]>CO>[CH:12]([NH:15][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][C:3]=1[S:8]([NH2:11])(=[O:10])=[O:9])([CH3:14])[CH3:13]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 6363IsopropylamineHCID 1184264-Chloro-3-pyridinesulphonamide

生成物 1

HCID 10632459HCID 10632459、化合物

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

10 g of 4-chloropyridine-3-sulfonamide are dissolved in 50 cm3 of methanol and 50 cm3 of isopropylamine. The solution is introduced into a sealed tube and brought to 120° C. for 18 hours. After cooling, the reaction mixture is concentrated to dryness under vacuum (rotary evaporator) and the residue is taken up in 200 cm3 of water. The precipitate corresponding to the title compound is collected on a filter and washed with water. The precipitate is redissolved in 100 cm3 of dilute NaOH. The solution is decolored with charcoal, filtered and then acidified to a pH of 6.5-7. The crystalline precipitate obtained is collected on a filter, washed with water and dried.

後処理

  1. additionThe solution is introduced into a sealed tube
  2. temperatureAfter cooling
  3. concentrationthe reaction mixture is concentrated to dryness under vacuum (rotary evaporator)
  4. customThe precipitate corresponding to the title compound is collected on
  5. filtrationa filter
  6. washwashed with water
  7. dissolutionThe precipitate is redissolved in 100 cm3 of dilute NaOH
  8. filtrationfiltered
  9. customThe crystalline precipitate obtained
  10. customis collected on a filter
  11. washwashed with water
  12. customdried

出典と根拠

ORDレコード
ord-03077c71aeb0444c961291f34c0c064d
出典データセット
uspto-grants-1995_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05459138

反応ノート

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