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Diphenylphosphinic chloride → HCID 70510866、化合物

HRID 1262883
ノート
印刷プレビュー

反応式

HRID 1262883 の反応式
C(N(C(C)C)CC)(C)C.C1(P(Cl)(C2C=CC=CC=2)=O)C=CC=CC=1.[C:25]([O:29][C:30]([N:32]([CH3:49])[C@H:33]([C:46](O)=[O:47])[CH2:34][C:35]1[CH:40]=[CH:39][C:38]([O:41][C:42]([CH3:45])([CH3:44])[CH3:43])=[CH:37][CH:36]=1)=[O:31])([CH3:28])([CH3:27])[CH3:26].Cl.[C:51]1([CH2:57][CH2:58][CH2:59][NH:60][C:61](=[O:68])[C@@H:62]([CH2:64][CH2:65][S:66][CH3:67])[NH2:63])[CH:56]=[CH:55][CH:54]=[CH:53][CH:52]=1>O1CCCC1>[C:25]([O:29][C:30]([N:32]([CH3:49])[C@H:33]([C:46]([NH:63][C@@H:62]([C:61]([NH:60][CH2:59][CH2:58][CH2:57][C:51]1[CH:52]=[CH:53][CH:54]=[CH:55][CH:56]=1)=[O:68])[CH2:64][CH2:65][S:66][CH3:67])=[O:47])[CH2:34][C:35]1[CH:40]=[CH:39][C:38]([O:41][C:42]([CH3:44])([CH3:45])[CH3:43])=[CH:37][CH:36]=1)=[O:31])([CH3:26])([CH3:27])[CH3:28]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 73910Diphenylphosphinic chlorideHCID 81531Diisopropylethylamine2 回HCID 54000823N-[(1,1-Dimethylethoxy)carbonyl]-O-(1,1-dimethylethyl)-N-methyl-L-tyrosineHCID 70510997HCID 70510997、化合物

生成物 1

HCID 70510866HCID 70510866、化合物

試薬・触媒・溶媒 1

HCID 8028
Tetrahydrofuran
溶媒
2 回

反応条件

温度
-20 °C

実験手順

Diisopropylethylamine (0.90 ml.), then diphenylphosphinyl chloride (1.23 g.), were added to a solution of N-(tert-butyloxycarbonyl)-O-(tert-butyl)-N-methyl-L-tyrosine (1.76 g.) in tetrahydrofuran (15 ml.) maintained at -20° C., and the mixture was stirred for ten minutes. A solution of N-(3-phenylpropyl)-D-methioninamide hydrochloride (1.58 g.) and diisopropylethylamine (0.90 ml.) in tetrahydrofuran (10 ml.) was then added. The mixture was stirred for one half hour at -20°, one hour at 0° C. and overnight at room temperature, then filtered and stripped of solvent. A solution of the residue in ethyl acetate (100 ml.) was washed with water, aqueous citric acid, water again, aqueous sodium bicarbonate and water again, dried and stripped of solvent. Purification of the residue by high pressure liquid chromatography on silica gel (350 g.) using hexane-ethyl acetate (2:1) as the eluant afforded in fractions 6-7 (k'=8-14) [N-(tert-butyloxycarbonyl)-O-(tert-butyl)-N-methyl-L-tyrosyl]-N-(3-phenylpropyl)-D-methioninamide as a clear gum (2.1 g.).

後処理

  1. stirringThe mixture was stirred for one half hour at -20°, one hour at 0° C. and overnight at room temperature
  2. filtrationfiltered
  3. washA solution of the residue in ethyl acetate (100 ml.) was washed with water, aqueous citric acid, water again
  4. dry with materialaqueous sodium bicarbonate and water again, dried
  5. customPurification of the residue by high pressure liquid chromatography on silica gel (350 g.)

出典と根拠

ORDレコード
ord-214dff10a3984679bf10cc884e0c0e85
出典データセット
uspto-grants-1984_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04454120

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート