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Ninhydrin → Benzyloxycarbonyl-L-valyl-L-leucyl-L-threonine methyl ester

HRID 1732518
ノート
印刷プレビュー

反応式

HRID 1732518 の反応式
[CH3:1][O:2][C:3](=[O:27])[C@H:4]([C@@H:24]([CH3:26])[OH:25])[NH:5][C:6](=[O:23])[C@H:7]([CH2:19][CH:20]([CH3:22])[CH3:21])[NH:8]C(OCC1C=CC=CC=1)=O.CCN(C(C)C)C(C)C.[N+](C1C=CC(O[C:47](=[O:63])[C@H:48]([CH:60]([CH3:62])[CH3:61])[NH:49][C:50]([O:52][CH2:53][C:54]2[CH:59]=[CH:58][CH:57]=[CH:56][CH:55]=2)=[O:51])=CC=1)([O-])=O.C1C=CC2N(O)N=NC=2C=1.C1C=C2C(C(O)(O)C(=O)C2=CC=1)=O>CCO.Cl.[Pd]>[CH3:1][O:2][C:3](=[O:27])[C@H:4]([C@@H:24]([CH3:26])[OH:25])[NH:5][C:6](=[O:23])[C@H:7]([CH2:19][CH:20]([CH3:22])[CH3:21])[NH:8][C:47](=[O:63])[C@H:48]([CH:60]([CH3:61])[CH3:62])[NH:49][C:50]([O:52][CH2:53][C:54]1[CH:55]=[CH:56][CH:57]=[CH:58][CH:59]=1)=[O:51]
参加物実験手順後処理出典と根拠反応ノート

参加物

9

反応物 5

HCID 10236NinhydrinHCID 757711-HydroxybenzotriazoleHCID 81531DiisopropylethylamineHCID 112124Z-Val-ONpHCID 54439782Benzyloxycarbonyl-L-leucyl-L-threonine methyl ester

生成物 1

HCID 53923485Benzyloxycarbonyl-L-valyl-L-leucyl-L-threonine methyl ester

試薬・触媒・溶媒 3

HCID 23938Palladium触媒HCID 313Hydrochloric Acid溶媒HCID 702Ethanol溶媒

実験手順

Benzyloxycarbonyl-L-leucyl-L-threonine methyl ester (I, 3.8 g, 10 mmole) was dissolved in a mixture of 95% EtOH (50 ml) and 1 N HCl (10 ml) and hydrogenated in the presence of a 10% Pd on charcoal catalyst (0.8 g). After removal of the catalyst and the solvent the residue was dissolved in DMF (35 ml), treated with DIEA (1.6 ml, 10 mmole), benzyloxycarbonyl-L-valine p-nitrophenyl ester (4.3 g, 12 mmole) and HOBt (1.5 g, 10 mmole). After a negative spot test with ninhydrin indicated the completion of the reaction, the solvent was removed in vacuo and the residue triturated with CHCl3 (40 ml). The resulting solid was washed with CHCl3 (20 ml) and dried: 4.5 g (94%, mp 217°-8° C.,) unchanged after extraction with solvents, [α]D24 -11.7° (c 1.5, DMF); RfC 0.75; Thr 1.08; Val 0.98; Leu 1.0.

後処理

  1. customAfter removal of the catalyst
  2. dissolutionthe solvent the residue was dissolved in DMF (35 ml)
  3. customthe completion of the reaction
  4. customthe solvent was removed in vacuo
  5. customthe residue triturated with CHCl3 (40 ml)
  6. washThe resulting solid was washed with CHCl3 (20 ml)
  7. customdried
  8. extraction4.5 g (94%, mp 217°-8° C.,) unchanged after extraction with solvents, [α]D24 -11.7° (c 1.5, DMF)

出典と根拠

ORDレコード
ord-065fcdcd96ec4e4f8d0f437e82a1a642
出典データセット
uspto-grants-1980_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04237046

反応ノート

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