Tetrahydrofuran → Methyl bis-(1-naphthylmethyl)acetyl-(alpha-methyl-D-tryptophan)

HRID 976038ノート

反応式

HRID 976038 の反応式
[CH3:1][NH:2][C@@:3]([CH3:17])([C:14]([OH:16])=[O:15])[CH2:4][C:5]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[NH:7][CH:6]=1.[C:18]1([CH2:28][CH:29]([CH2:33][C:34]2[C:43]3[C:38](=[CH:39][CH:40]=[CH:41][CH:42]=3)[CH:37]=[CH:36][CH:35]=2)[C:30](Cl)=O)[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[CH:21]=[CH:20][CH:19]=1.CCN(CC)CC.C1C[O:54]CC1>>[CH3:30][C:29]([CH2:33][C:34]1[C:43]2[C:38](=[CH:39][CH:40]=[CH:41][CH:42]=2)[CH:37]=[CH:36][CH:35]=1)([CH2:28][C:18]1[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[CH:21]=[CH:20][CH:19]=1)[C:1]([NH:2][C@@:3]([CH3:17])([C:14]([OH:16])=[O:15])[CH2:4][C:5]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[NH:7][CH:6]=1)=[O:54]

参加物

5

実験手順

A solution of 2.0 g (8.6 mmol) of methyl α-methyl-D-tryptophan in 30 mL THF was treated with 3.09 g (8.6 mmol) of bis-(1-naphthylmethyl)acetyl chloride (J. Med. Chem., 35:1032 (1992)) followed by 1.2 mL (8.6 mmol) of Et3N. After stirring at room temperature for 2 days, the solvent was removed under reduced pressure and the residue taken up in EtOAc and washed with 1HCl, H2O, saturated NaHCO3, and saturated NaCl. Drying over MgSO4 and removal of the solvent under reduced pressure gave 4.77 g of the crude product. Recrystallization from CH3CN/H2O gave 4.24 g (88.9% yield) of the product as a cream solid, mp 193°-195° C. The structure was confirmed by NMR and mass spectroscopy.

後処理

  1. customthe solvent was removed under reduced pressure
  2. washwashed with 1HCl, H2O, saturated NaHCO3, and saturated NaCl
  3. dry with materialDrying over MgSO4 and removal of the solvent under reduced pressure
  4. customgave 4.77 g of the crude product
  5. customRecrystallization from CH3CN/H2O

出典と根拠

ORDレコード
ord-7ed07fbcda7a47d681ad90327e7f0d90
出典データセット
uspto-grants-1997_03
特許番号
US05610177

反応ノート

読み込み中…