Sodium triacetoxyborohydride → 2-{2-[(Adamantan-1-ylmethyl)-amino]4-bromo-phenyl}-malonic acid di-tert-butyl ester

HRID 1355670ノート

反応式

HRID 1355670 の反応式
[C:1]12([CH:11]=O)[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH2:2]1)[CH2:8]2.[C:13]([O:17][C:18](=[O:35])[CH:19]([C:27]1[CH:32]=[CH:31][C:30]([Br:33])=[CH:29][C:28]=1[NH2:34])[C:20]([O:22][C:23]([CH3:26])([CH3:25])[CH3:24])=[O:21])([CH3:16])([CH3:15])[CH3:14].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>C(O)(=O)C>[C:13]([O:17][C:18](=[O:35])[CH:19]([C:27]1[CH:32]=[CH:31][C:30]([Br:33])=[CH:29][C:28]=1[NH:34][CH2:11][C:1]12[CH2:10][CH:5]3[CH2:4][CH:3]([CH2:9][CH:7]([CH2:6]3)[CH2:8]1)[CH2:2]2)[C:20]([O:22][C:23]([CH3:26])([CH3:25])[CH3:24])=[O:21])([CH3:14])([CH3:15])[CH3:16]

参加物

5

実験手順

To a solution of adamantane-1-carbaldehyde (3.77 g, 23 mmol) in acetic acid (45 ml) was added 2-(2-amino-4-bromo-phenyl)-malonic acid di-tert-butyl ester (4.44 g, 11.5 mmol) followed by addition of sodium triacetoxyborohydride (3.41 g, 16 mmol). The reaction mixture stirred for 30 minutes. After removal of the acetic acid, the reaction mixture was then partitioned between water and chloroform. Powdered K2CO3 was added and the pH of the aqueous layer was adjusted to 8. After separation, the organic layer was then washed with brine, dried over MgSO4, filtered and concentrated under vacuum to give the crude title compound of 9A as a brown oil (7.81 9), which was used in the next step without further purification.

後処理

  1. customAfter removal of the acetic acid
  2. customthe reaction mixture was then partitioned between water and chloroform
  3. additionPowdered K2CO3 was added
  4. customAfter separation
  5. washthe organic layer was then washed with brine
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated under vacuum

出典と根拠

ORDレコード
ord-0c59108801aa4252b7e40e264ab3cfb2
出典データセット
uspto-grants-2003_07
特許番号
US06586447B1

反応ノート

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