Ethylmorpholine → Z-Ile-Phe-OBut

HRID 904956

反応式

HRID 904956 の反応式
C(N1CCOCC1)C.[NH:9]([C:18]([O:20][CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)=[O:19])[C@H:10]([C:15]([OH:17])=O)[C@H:11]([CH2:13][CH3:14])[CH3:12].[NH2:28][C@H:29]([C:37]([O:39][C:40]([CH3:43])([CH3:42])[CH3:41])=[O:38])[CH2:30][C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1.C1C=CC2N(O)N=NC=2C=1.C1CCC(N=C=NC2CCCCC2)CC1>CN(C)C=O>[NH:9]([C:18]([O:20][CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)=[O:19])[C@H:10]([C:15]([NH:28][C@H:29]([C:37]([O:39][C:40]([CH3:43])([CH3:42])[CH3:41])=[O:38])[CH2:30][C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1)=[O:17])[C@H:11]([CH2:13][CH3:14])[CH3:12]

参加物

7

実験手順

1.3 ml of N-ethylmorpholine are added to the solution of 2.65 g of Z-Ile-OH, 2.58 g of H-Phe-OBut and 1.35 g of HOBt in 30 ml of dimethylformamide and 2.2 g of DCC are added to 0° C. The mixture is allowed to stand for 1 hour at 0° C. and overnight at room temperature. On the following day the precipitate is filtered off and the filtrate is concentrated. The residue is partitioned between ethyl acetate and water. The ethyl acetate phase is extracted by shaking with 20 ml of saturated NaHCO3 solution, 20 ml of K2SO4 /KHSO4 solution and 20 ml of NaHCO3 solution and is dried over Na2SO4 and concentrated. The product crystallizes from petroleum ether. Yield 3.7 g, melting point 122°-125°.

後処理

  1. additionare added to 0° C
  2. filtrationOn the following day the precipitate is filtered off
  3. concentrationthe filtrate is concentrated
  4. customThe residue is partitioned between ethyl acetate and water
  5. extractionThe ethyl acetate phase is extracted
  6. dry with materialis dried over Na2SO4
  7. concentrationconcentrated
  8. customThe product crystallizes from petroleum ether

出典と根拠

ORDレコード
ord-a9eaf38e2fd04680b6ed72562a431c04
出典データセット
uspto-grants-1983_12
特許番号
US04420424

関連ノート

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