Sodium Hydroxide → 4-(2-tert-Butoxycarbonylamino-2-cyclohexyl-acetyl)-1-cyclopropanecarbonyl-octahydro-pyrrolo[3,2-b]pyrrole-3-carboxylic acid

HRID 446981ノート

反応式

HRID 446981 の反応式
C[O:2][C:3]([CH:5]1[CH2:9][N:8]([C:10]([CH:12]2[CH2:14][CH2:13]2)=[O:11])[CH:7]2[CH2:15][CH2:16][N:17]([C:18](=[O:34])[CH:19]([NH:26][C:27]([O:29][C:30]([CH3:33])([CH3:32])[CH3:31])=[O:28])[CH:20]3[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]3)[CH:6]12)=[O:4].[OH-].[Na+]>CO>[C:30]([O:29][C:27]([NH:26][CH:19]([CH:20]1[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]1)[C:18]([N:17]1[CH:6]2[CH:7]([N:8]([C:10]([CH:12]3[CH2:13][CH2:14]3)=[O:11])[CH2:9][CH:5]2[C:3]([OH:4])=[O:2])[CH2:15][CH2:16]1)=[O:34])=[O:28])([CH3:33])([CH3:31])[CH3:32]

参加物

4

実験手順

A solution of 44 (580 mg, 1.21 mmol) in MeOH (20 mL) was treated with 1M NaOH (4 mL) at ambient temperature. After 4 h, the solution was concentrated and diluted with EtOAc and 1M HCl. The layers were separated and the aqueous phase was extracted with EtOAc. The combined organic extracts were washed successively with 1M HCl, and brine, dried over anhydrous Na2SO4, filtered and concentrated to afford 45 (613 mg) as a yellow-colored foam which was used without further purification. Mass spectrum, m/z [464.6] (M+H)+.

後処理

  1. concentrationthe solution was concentrated
  2. additiondiluted with EtOAc and 1M HCl
  3. customThe layers were separated
  4. extractionthe aqueous phase was extracted with EtOAc
  5. washThe combined organic extracts were washed successively with 1M HCl, and brine
  6. dry with materialdried over anhydrous Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-ebfc484d18ba42c5a005b916bbe3611a
出典データセット
uspto-grants-2013_07
特許番号
US08481495B2

反応ノート

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