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

HRID 1732518
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HRID 1732518 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

9

반응물 5

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

생성물 1

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

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 313Hydrochloric Acid용매HCID 702Ethanol용매

실험 절차

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.

후처리

  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)

출처 및 근거

ORD 기록
ord-065fcdcd96ec4e4f8d0f437e82a1a642
출처 데이터셋
uspto-grants-1980_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04237046

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