2-Propanethiol → 2-Isopropylsulfanyl-6-methyl-nicotinic acid methyl ester

HRID 62848

反応式

HRID 62848 の反応式
[CH3:1][O:2][C:3](=[O:12])[C:4]1[CH:9]=[CH:8][C:7]([CH3:10])=[N:6][C:5]=1Cl.C([O-])([O-])=O.[Cs+].[Cs+].[CH3:19][CH:20]([SH:22])[CH3:21]>CN(C=O)C>[CH3:1][O:2][C:3](=[O:12])[C:4]1[CH:9]=[CH:8][C:7]([CH3:10])=[N:6][C:5]=1[S:22][CH:20]([CH3:21])[CH3:19]

参加物

5

反応物 3

HCID 63642-PropanethiolHCID 10796Cesium carbonateHCID 13055804Methyl 2-chloro-6-methylpyridine-3-carboxylate

生成物 1

HCID 901181052-Isopropylsulfanyl-6-methyl-nicotinic acid methyl ester収率 69.8%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

2-Chloro-6-methyl-nicotinic acid methyl ester (1.39 g, 7.44 mmol) obtained in Step A was dissolved in DMF (15 mL). Cs2CO3(4.88 g, 14.99 mmol) and propane-2-thiol (1.39 mL, 14.99 mmol) were added to the solution, and the mixture was stirred at room temperature for 2 hours. The reactant was concentrated under reduced pressure to remove the solvent. The residue was added with water and then extracted with EtOAc. The organic layer was dried with MgSO4, filtered and concentrated under reduced pressure. The obtained residue was purified by column chromatography (eluent EtOAc/Hex=1/5) to obtain the title compound (1.17 g, 69%).

後処理

  1. concentrationThe reactant was concentrated under reduced pressure
  2. customto remove the solvent
  3. additionThe residue was added with water
  4. extractionextracted with EtOAc
  5. dry with materialThe organic layer was dried with MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customThe obtained residue was purified by column chromatography (eluent EtOAc/Hex=1/5)

出典と根拠

ORDレコード
ord-7ad44a8f9f314848acf3a650ee093685
出典データセット
uspto-grants-2016_09
特許番号
US09447044B2

関連ノート

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