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Sodium Chloride → 4-Methyl-2-(pyridin-3-yl)-1,3-thiazole-5-amine

HRID 1182777
ノート
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反応式

HRID 1182777 の反応式
[CH3:1][C:2]1[N:3]=[C:4]([C:10]2[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=2)[S:5][C:6]=1[N+:7]([O-])=O.[Sn](Cl)Cl.C(OC)(C)(C)C.[Cl-].[Na+]>Cl.C(OCC)(=O)C>[CH3:1][C:2]1[N:3]=[C:4]([C:10]2[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=2)[S:5][C:6]=1[NH2:7]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 5234Sodium ChlorideHCID 15413tert-Butyl methyl etherHCID 24479Stannous ChlorideHCID 2176783-(4-Methyl-5-nitro-1,3-thiazol-2-yl)pyridine

生成物 1

HCID 666453454-Methyl-2-(pyridin-3-yl)-1,3-thiazole-5-amine

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid溶媒3 回
HCID 8857Ethyl Acetate溶媒

実験手順

10.1 g (45.6 mmol) of 3-(4-methyl-5-nitro-1,3-thiazol-2-yl)pyridine (for preparation see DE 2221647) were dissolved in 100 ml of 10% hydrochloric acid together with 10 ml of conc. hydrochloric acid, and 25 g of tin(II) chloride dissolved in 10% hydrochloric acid were added in portions, and the mixture was stirred for 1 h (hour), in the course of which heating occurred. The mixture was poured into ice/sodium hydroxide solution, methyl t-butyl ether, ethyl acetate and saturated sodium chloride solution were added, the mixture was extracted 4 times at pH=10 with ethyl acetate, the combined organic phases were dried with Mg504 and the mixture was concentrated. The residue was recrystallized from benzotrifluoride.

後処理

  1. additionwere added in portions
  2. temperaturein the course of which heating
  3. additionwere added
  4. extractionthe mixture was extracted 4 times at pH=10 with ethyl acetate
  5. customthe combined organic phases were dried with Mg504
  6. concentrationthe mixture was concentrated
  7. customThe residue was recrystallized from benzotrifluoride

出典と根拠

ORDレコード
ord-9806e7f9369644d3860d55efa75ff097
出典データセット
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08664229B2

反応ノート

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