Sodium Hydroxide → HCID 54048888、化合物

HRID 372776ノート

反応式

HRID 372776 の反応式
C([O:8][C:9](=[O:57])[C@H:10]([CH2:53][CH2:54][S:55][CH3:56])[NH:11][C:12](=[O:52])[C@H:13]([CH2:42][C:43]1[C:51]2[C:46](=[CH:47][CH:48]=[CH:49][CH:50]=2)[NH:45][CH:44]=1)[NH:14][C:15](=[O:41])[CH2:16][NH:17][C:18](=[O:40])[CH2:19][NH:20][C:21](=[O:39])[C@H:22]([CH2:31][C:32]1[CH:37]=[CH:36][C:35]([OH:38])=[CH:34][CH:33]=1)[NH:23][C:24]([O:26][C:27]([CH3:30])([CH3:29])[CH3:28])=[O:25])C1C=CC=CC=1.[OH-].[Na+]>CO>[C:27]([O:26][C:24]([NH:23][C@H:22]([C:21]([NH:20][CH2:19][C:18]([NH:17][CH2:16][C:15]([NH:14][C@H:13]([C:12]([NH:11][C@H:10]([C:9]([OH:57])=[O:8])[CH2:53][CH2:54][S:55][CH3:56])=[O:52])[CH2:42][C:43]1[C:51]2[C:46](=[CH:47][CH:48]=[CH:49][CH:50]=2)[NH:45][CH:44]=1)=[O:41])=[O:40])=[O:39])[CH2:31][C:32]1[CH:33]=[CH:34][C:35]([OH:38])=[CH:36][CH:37]=1)=[O:25])([CH3:30])([CH3:28])[CH3:29]

参加物

4

反応条件

温度
10 °C

実験手順

21.1 Parts N-t-butoxycarbonyl-L-tyrosylglycylglycyl-L-tryptophyl-L-methionine benzyl ester is dissolved in 70 parts methanol and the solution cooled to 10° C. Then, 90 parts by volume of 1 N sodium hydroxide solution is added dropwise with stirring while maintaining the temperature below 20° C. After standing at room temperature for 1 hour, the methanol is removed by evaporation under reduced pressure. The solution is washed once with ethyl ether to remove benzyl alcohol and the aqueous layer acidified with 90 parts by volume 1 N hydrochloric acid. The solid which results is filtered and washed with water to afford N-t-butoxycarbonyl-L-tyrosylglycylglycyl-L-tryptophyl-L-methionine.

後処理

  1. temperaturewhile maintaining the temperature below 20° C
  2. customthe methanol is removed by evaporation under reduced pressure
  3. washThe solution is washed once with ethyl ether
  4. customto remove benzyl alcohol
  5. customThe solid which results
  6. filtrationis filtered
  7. washwashed with water

出典と根拠

ORDレコード
ord-c362007cee2146d6aeb8de4b239eb2e1
出典データセット
uspto-grants-1978_05
特許番号
US04092304

反応ノート

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