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

HRID 444472
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HRID 444472 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

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

생성물 1

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

시약·촉매·용매 2

HCID 23978Copper촉매HCID 887Methanol용매

실험 절차

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.

후처리

  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.

출처 및 근거

ORD 기록
ord-5b40d5c1b2344b7d891aefd799c3405e
출처 데이터셋
uspto-grants-1981_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04264605

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