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Nalpha-t-butoxycarbonyl-D-valine p-nitrophenyl ester → HCID 178465160、化合物

HRID 1763736
ノート
印刷プレビュー

反応式

HRID 1763736 の反応式
[ClH:1].C(NC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(OCC1C=CC=CC=1)=O)C.Cl.Cl.[CH2:43]([NH:45][C:46](=[O:71])[C@@H:47]1[CH2:51][CH2:50][CH2:49][N:48]1[C:52](=[O:70])[C@H:53]([CH2:63][CH2:64][CH2:65][NH:66][C:67](=[NH:69])[NH2:68])[NH:54][C:55](=[O:62])[C@H:56]([CH2:58][CH:59]([CH3:61])[CH3:60])[NH2:57])[CH3:44].[N+](C1C=CC([O:81][C:82](=O)[C@@H:83]([CH:92]([CH3:94])[CH3:93])[NH:84][C:85]([O:87][C:88]([CH3:91])([CH3:90])[CH3:89])=[O:86])=CC=1)([O-])=O>CN(C)C=O>[ClH:1].[CH2:43]([NH:45][C:46](=[O:71])[C@@H:47]1[CH2:51][CH2:50][CH2:49][N:48]1[C:52](=[O:70])[C@H:53]([CH2:63][CH2:64][CH2:65][NH:66][C:67](=[NH:68])[NH2:69])[NH:54][C:55](=[O:62])[C@H:56]([CH2:58][CH:59]([CH3:60])[CH3:61])[NH:57][C:82](=[O:81])[C@@H:83]([CH:92]([CH3:93])[CH3:94])[NH:84][C:85]([O:87][C:88]([CH3:89])([CH3:90])[CH3:91])=[O:86])[CH3:44]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 22804944Nalpha-t-butoxycarbonyl-D-valine p-nitrophenyl esterHCID 178465162HCID 178465162、化合物HCID 178465165HCID 178465165、化合物

生成物 1

HCID 178465160HCID 178465160、化合物

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

Nα -t-butoxycarbonyl-D-valyl-L-leucyl-L-arginyl-L-proline N-ethylamide hydrochloride is prepared from 3.8 g., 6.5 mmol, of Nα -benzyloxycarbonyl-L-leucyl-L-arginyl-L-proline N-ethylamide hydrochloride by de-protection by the hydrogenation procedure as described in Example 2, to yield 2.9 g., 6.5 mmol, of L-leucyl-L-arginyl-L-proline N-ethylamide dihydrochloride as a glassy solid. This material is dissolved in 25 ml. of dimethylformamide and treated with 2.2 g., 6.5 mmol, of Nα -t-butoxycarbonyl-D-valine p-nitrophenyl ester. The reaction is held at room temperature for four days and is then evaporated to dryness under reduced pressure. The residue is dissolved in 10 ml. of methanol and the product precipitated by the addition of 500 ml. of anhydrous ether. The solid product is purified by chromatography over silica gel with toluene-methanol (70:30); 1.1 g.; [α]D23 -53.5° (c 1.0, methanol).

後処理

  1. customto yield 2.9 g
  2. dissolutionThis material is dissolved in 25 ml
  3. customis then evaporated to dryness under reduced pressure
  4. dissolutionThe residue is dissolved in 10 ml
  5. customof methanol and the product precipitated by the addition of 500 ml
  6. customThe solid product is purified by chromatography over silica gel with toluene-methanol (70:30)

出典と根拠

ORDレコード
ord-f257323c82ce4b26a3b9367a5576e8cb
出典データセット
uspto-grants-1978_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04111923

反応ノート

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