Hydrochloric Acid → HCID 68814989、化合物

HRID 1436608ノート

反応式

HRID 1436608 の反応式
C[O:2][C:3](=[O:21])[C:4]1[CH:9]=[C:8]([N:10]([CH3:14])[CH2:11][CH2:12][CH3:13])[N:7]=[C:6]([N:15]([S:17]([CH3:20])(=[O:19])=[O:18])[CH3:16])[CH:5]=1.[OH-].[Li+].Cl>C1COCC1>[CH3:20][S:17]([N:15]([CH3:16])[C:6]1[CH:5]=[C:4]([CH:9]=[C:8]([N:10]([CH3:14])[CH2:11][CH2:12][CH3:13])[N:7]=1)[C:3]([OH:21])=[O:2])(=[O:18])=[O:19]

参加物

5

実験手順

Dissolve 2-(methanesulfonyl-methylamino)-6-(methylpropylamino)-isonicotinic acid methyl ester (796 mg, 2.52 mmoles) in THF (35 mL) and add 1 N lithium hydroxide (12.6 mL). Stir at room temperature for 16 h, acidify with 5 N HCl (2.6 mL), and partition between diethyl ether and water. Wash the diethyl ether layer with saturated aqueous sodium chloride, dry (magnesium sulfate) and concentrate to give the title compound as a yellow solid (650 mg, 85%).

後処理

  1. custompartition between diethyl ether and water
  2. washWash the diethyl ether layer with saturated aqueous sodium chloride
  3. dry with materialdry (magnesium sulfate)
  4. concentrationconcentrate

出典と根拠

ORDレコード
ord-ef7f5926b5b54e2e8ca6b4c69826ad85
出典データセット
uspto-grants-2009_11
特許番号
US07618978B2

反応ノート

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