Sodium Hydroxide → HCID 44599428、化合物

HRID 510799ノート

反応式

HRID 510799 の反応式
[CH3:1][O:2][C:3]1[CH:36]=[C:35]([CH:37]2[CH2:39][CH2:38]2)[CH:34]=[CH:33][C:4]=1[CH2:5][CH2:6][NH:7][C:8]([C:10]1[CH:32]=[CH:31][C:13]([O:14][C:15]2[CH:24]=[C:23]3[C:18]([CH:19]([C:25]([O:27]CC)=[O:26])[CH2:20][CH2:21][O:22]3)=[CH:17][C:16]=2[Cl:30])=[CH:12][CH:11]=1)=[O:9].[OH-].[Na+]>C1COCC1.C(O)C.CCOC(C)=O.Cl>[Cl:30][C:16]1[CH:17]=[C:18]2[C:23](=[CH:24][C:15]=1[O:14][C:13]1[CH:31]=[CH:32][C:10]([C:8](=[O:9])[NH:7][CH2:6][CH2:5][C:4]3[CH:33]=[CH:34][C:35]([CH:37]4[CH2:39][CH2:38]4)=[CH:36][C:3]=3[O:2][CH3:1])=[CH:11][CH:12]=1)[O:22][CH2:21][CH2:20][CH:19]2[C:25]([OH:27])=[O:26]

参加物

7

実験手順

To a stirred solution of ethyl 7-(4-(2-methoxy-4-cyclopropylphenethylcarbamoyl)phenoxy)-6-chlorochroman-4-carboxylate (0.07 g; 0.133 mmol) in a mixture of 1.2 mL THF and 0.6 mL ethanol at ambient temperature was added 0.53 mL of 1M aqueous NaOH. The resulting slightly cloudy mixture was vigorously stirred at ambient temperature. After 1 hour the reaction mixture was diluted with 6 mL EtOAc and 3 mL of 1M aqueous HCl, then transferred to a separatory funnel. After shaking, the organic layer was washed with 2 mL brine, then dried over sodium sulfate and evaporated to give 62 mg of 6-chloro-7-(4-(4-cyclopropyl-2-methoxyphenethylcarbamoyl)phenoxy)chroman-4-carboxylic acid as a colorless oil. MS (apci, pos) m/z=523.

後処理

  1. customtransferred to a separatory funnel
  2. stirringAfter shaking
  3. washthe organic layer was washed with 2 mL brine
  4. dry with materialdried over sodium sulfate
  5. customevaporated

出典と根拠

ORDレコード
ord-b8a6c64968d3455cade3378992ba2537
出典データセット
uspto-grants-2015_08
特許番号
US09096567B2

反応ノート

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