Water → 1-Methyl-5-(4-pyridinylamino)-1H-indole

HRID 484065

反応式

HRID 484065 の反応式
Cl.Cl[C:3]1[CH:8]=[CH:7][N:6]=[CH:5][CH:4]=1.[NH2:9][C:10]1[CH:11]=[C:12]2[C:16](=[CH:17][CH:18]=1)[N:15]([CH3:19])[CH:14]=[CH:13]2.O.C(=O)([O-])[O-].[Na+].[Na+]>CN1CCCC1=O>[CH3:19][N:15]1[C:16]2[C:12](=[CH:11][C:10]([NH:9][C:3]3[CH:8]=[CH:7][N:6]=[CH:5][CH:4]=3)=[CH:18][CH:17]=2)[CH:13]=[CH:14]1

参加物

6

反応物 4

HCID 962WaterHCID 10340Sodium CarbonateHCID 818524-Chloropyridine hydrochloride2 回HCID 27695641-methyl-1H-indol-5-amine

生成物 1

HCID 98159221-Methyl-5-(4-pyridinylamino)-1H-indole収率 53.3%

試薬・触媒・溶媒 1

HCID 13387N-methyl-2-pyrrolidone溶媒

実験手順

4-Chloropyridine hydrochloride (8 g) was added to a solution of 5-amino-1-methylindole (7 g) in 75 ml 1 -methyl-2-pyrrolidinone preheated to 100° C. The addition of 4-chloropyridine hydrochloride (4 g) after one hour caused no further reaction as determined by TLC. After two hours the reaction mixture was cooled, stirred with water, basified with sodium carbonate and extracted with ethyl acetate. The dried (anhydrous magnesium sulfate) organic layer was filtered and evaporated to 12.7 g of an oil. The oil was eluted through silica with 10% methanol in dichloromethane via flash column chromatography to give the product which was triturated with ether to yield 5.7 g of a solid, m.p. 202°-203° C. Recrystallization from acetonitrile yielded 5 g of product as crystals, mp 209°-211° C.

後処理

  1. custompreheated to 100° C
  2. customno further reaction
  3. temperatureAfter two hours the reaction mixture was cooled
  4. extractionextracted with ethyl acetate
  5. dry with materialThe dried (anhydrous magnesium sulfate) organic layer
  6. filtrationwas filtered
  7. customevaporated to 12.7 g of an oil
  8. washThe oil was eluted through silica with 10% methanol in dichloromethane via flash column chromatography
  9. customto give the product which
  10. customwas triturated with ether

出典と根拠

ORDレコード
ord-31ed6e26f1c54ae7b4ee7c327a873d13
出典データセット
uspto-grants-1993_07
特許番号
US05229401

関連ノート

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