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p-Chlorothiophenol → 5-[(4-Chlorophenyl)sulfanyl]pyridin-2-amine

HRID 444472
ノート
印刷プレビュー

反応式

HRID 444472 の反応式
[NH2:1][C:2]1[CH:7]=[CH:6][C:5](Br)=[CH:4][N:3]=1.[Cl:9][C:10]1[CH:15]=[CH:14][C:13]([SH:16])=[CH:12][CH:11]=1.C[O-].[Na+]>[Cu].CO>[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([S:16][C:13]2[CH:14]=[CH:15][C:10]([Cl:9])=[CH:11][CH:12]=2)=[CH:4][N:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 7815p-ChlorothiophenolHCID 706222-Amino-5-bromopyridineHCID 10942334Sodium Methoxide

生成物 1

HCID 129127435-[(4-Chlorophenyl)sulfanyl]pyridin-2-amine

試薬・触媒・溶媒 2

HCID 23978Copper触媒HCID 887Methanol溶媒

実験手順

2-Amino-5-bromopyridine (7.8 grams), 4-chlorothiophenol (9.2 grams), sodium methoxide (3.5 grams), and copper powder (1.0 gram) were reacted in 100 ml. of methanol, for 12 hours, in a bomb, in accordance with the procedures of J. Med. Chem. 21, 235 (1978). The reaction mixture was filtered, washed with methanol, and methanol removed by evaporation. The methanol washes were combined with ethyl acetate extracts of solids made after refluxing on a steam bath for one hour. Solvents were removed and the solids dissolved in ethyl acetate and filtered to remove insolubles. The liquid was passed over a silica column with ethyl acetate, and the fraction corresponding to the product amine (Rf ≅0.2) collected., yield 6.5 grams, m.p., 161°-163° C.

後処理

  1. filtrationThe reaction mixture was filtered
  2. washwashed with methanol, and methanol
  3. customremoved by evaporation
  4. temperatureafter refluxing on a steam bath for one hour
  5. customSolvents were removed
  6. dissolutionthe solids dissolved in ethyl acetate
  7. filtrationfiltered
  8. customto remove insolubles
  9. customthe fraction corresponding to the product amine (Rf ≅0.2) collected
  10. customm.p., 161°-163° C.

出典と根拠

ORDレコード
ord-5b40d5c1b2344b7d891aefd799c3405e
出典データセット
uspto-grants-1981_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04264605

反応ノート

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