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Pentachlorophenol → Ethyl ((benzyloxy)carbonyl)-L-phenylalanylglycinate

HRID 1287254
ノート
印刷プレビュー

反応式

HRID 1287254 の反応式
[C:1]([NH:11][C@H:12]([C:20]([OH:22])=O)[CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)([O:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:2].ClC1C(O)=C(Cl)C(Cl)=C(Cl)C=1Cl.C([N+]#[C-])(C)C.Cl.[CH2:41]([O:43][C:44](=[O:47])[CH2:45][NH2:46])[CH3:42]>C(Cl)(Cl)Cl.C(N(CC)CC)C>[CH2:41]([O:43][C:44](=[O:47])[CH2:45][NH:46][C:20](=[O:22])[C@H:12]([CH2:13][C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1)[NH:11][C:1]([O:3][CH2:4][C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1)=[O:2])[CH3:42]
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 4

HCID 992PentachlorophenolHCID 70878Benzyloxycarbonyl-L-phenylalanineHCID 150783Isopropyl isocyanideHCID 2723640Glycine ethyl ester, hydrochloride

生成物 1

HCID 12628842Ethyl ((benzyloxy)carbonyl)-L-phenylalanylglycinate収率 82%

試薬・触媒・溶媒 2

HCID 6212
Chloroform
溶媒
2 回
HCID 8471Triethylamine溶媒

反応条件

温度
50 °C

実験手順

A solution of 6.0 (20 mM) N-carbobenzoxy-L-phenylalanine, 5.3 g (20 mM) pentachlorophenol, and 2.0 g (30 mM) isopropyl isonitrile in 40 ml chloroform was mixed with a solution of 2.8 g (20 mM) glycine ethyl ester hydrochloride and 2.02 g (20 mM) triethylamine in 30 ml chloroform. The mixture was heated at 50°C for 24 hours and evaporated. The residue was taken up in 150 ml ethyl acetate. The solution was washed sequentially with 100 ml water, 120 ml 1-N hydrochloric acid, 4 times 120 ml 5% sodium bicarbonate solution, and again with 100 ml water, then dried with desiccated sodium sulfate and evaporated. When the residue was crystallized from ethyl acetate and petroleum ether, 6.3 g N-carbobenzoxy-L-phenylalanyl-glycine ethyl ester was obtained (82% yield). Recrystallizing from ethyl acetate and petroleum ether reduced the yield to 5.4 g (70%). M.P. 107° - 108.5° C. [ α]D25 = - 17.1° (C = 2, in ethanol).

後処理

  1. customevaporated
  2. washThe solution was washed sequentially with 100 ml water, 120 ml 1-N hydrochloric acid, 4 times 120 ml 5% sodium bicarbonate solution
  3. dry with materialagain with 100 ml water, then dried with desiccated sodium sulfate
  4. customevaporated
  5. customWhen the residue was crystallized from ethyl acetate and petroleum ether

出典と根拠

ORDレコード
ord-8eac8905b27c4eef9c3dbe86bcbb6138
出典データセット
uspto-grants-1976_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03984417

反応ノート

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