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4-Methylmorpholine → N-[1-(2-t-Butyloxycarbonyl-3-dibenzylaminopropyl)-1-cyclopentane-carbonyl]-O-t-butyl-(S)-tyrosine-t-butyl ester

HRID 1110460
ノート
印刷プレビュー

反応式

HRID 1110460 の反応式
[C:1]([O:5][C:6]([CH:8]([CH2:18][N:19]([CH2:27][C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)[CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[CH2:9][C:10]1([C:15]([OH:17])=O)[CH2:14][CH2:13][CH2:12][CH2:11]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].ON1C2C=C[CH:42]=[CH:43][C:38]=2N=N1.[CH2:44](N=C=NCCCN(C)C)C.[C:55]([O:59][C:60](=[O:75])[C@H:61]([CH2:63][C:64]1[CH:69]=[CH:68][C:67]([OH:70])=[CH:66][C:65]=1C(C)(C)C)[NH2:62])([CH3:58])([CH3:57])[CH3:56].CN1CCOCC1>ClCCl>[C:55]([O:59][C:60](=[O:75])[C@H:61]([CH2:63][C:64]1[CH:65]=[CH:66][C:67]([O:70][C:43]([CH3:42])([CH3:38])[CH3:44])=[CH:68][CH:69]=1)[NH:62][C:15]([C:10]1([CH2:9][CH:8]([C:6]([O:5][C:1]([CH3:4])([CH3:2])[CH3:3])=[O:7])[CH2:18][N:19]([CH2:27][C:28]2[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=2)[CH2:20][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[CH2:14][CH2:13][CH2:12][CH2:11]1)=[O:17])([CH3:56])([CH3:57])[CH3:58]
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

7

反応物 5

HCID 79724-MethylmorpholineHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 757711-HydroxybenzotriazoleHCID 221554593-(1-Carboxycyclopentyl)-2(dibenzylaminomethyl)propanoic acid t-butyl esterHCID 573028330-t-Butyltyrosine t-butyl ester

生成物 1

HCID 54036042
N-[1-(2-t-Butyloxycarbonyl-3-dibenzylaminopropyl)-1-cyclopentane-carbonyl]-O-t-butyl-(S)-tyrosine-t-butyl ester
収率 5,768.4%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

To an ice cold solution of 1-(2-t-butyloxycarbonyl-3-dibenzylaminopropyl)-1-cyclopentane carboxylic acid (12.7 g, 27 mmole) in dry dichloromethane (100 ml) was added 1-hydroxybenztriazole (4.2 g,.31 mmole), and 1-ethyl-3-(dimethylaminopropyl)-carbodiimide (7 g, 36 mmole) and the resulting solution stirred at 0° C. for 30 minutes. To this solution was added 0-t-butyltyrosine t-butyl ester (8.4 g, 28.6 mmole) and N-methylmorpholine (5.25 g, 52 mmole) and the solution allowed to stand overnight at room temperature. The solvent was evaporated under reduced pressure and the resultant mobile oil was dissolved in methylene chloride and washed with water (2 x ), 2M hydrochloric acid and saturated aqueous sodium bicarbonate (1 x) dried (MgSO4), and the solution filtered and evaporated to yield the crude product as a gum. Recrystallization from n-hexane gave the title compound as a solid (13 g, 69%), m.p. 82-87° C. A further batch of material was obtained by evaporation of the supernatant liquors and further recrystallisation. Found: C,74.12; H,8.69; N,3.87. C45H62N2O6 requires C,74.34; H,8.59; N,3.85%.

後処理

  1. waitto stand overnight at room temperature
  2. customThe solvent was evaporated under reduced pressure
  3. dissolutionthe resultant mobile oil was dissolved in methylene chloride
  4. washwashed with water (2 x ), 2M hydrochloric acid and saturated aqueous sodium bicarbonate (1 x)
  5. dry with materialdried (MgSO4)
  6. filtrationthe solution filtered
  7. customevaporated
  8. customto yield the crude product as a gum
  9. customRecrystallization from n-hexane

出典と根拠

ORDレコード
ord-fdce5d5343454896af4d0210372ca2a1
出典データセット
uspto-grants-1990_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04975444

反応ノート

読み込み中…

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