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4-Methylmorpholine → (2S,4S)-4-acetylthio-1-(4-nitrobenzyloxycarbonyl)-2-(3-(4-nitrobenzyloxycarbonylmethylaminocarbonyl)phenylcarbamoyl)-pyrrolidine

HRID 260314
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 260314
[C:1]([S:4][C@@H:5]1[CH2:9][N:8]([C:10]([O:12][CH2:13][C:14]2[CH:19]=[CH:18][C:17]([N+:20]([O-:22])=[O:21])=[CH:16][CH:15]=2)=[O:11])[C@H:7]([C:23](=[O:34])[NH:24][C:25]2[CH:30]=[CH:29][CH:28]=[C:27]([C:31]([OH:33])=O)[CH:26]=2)[CH2:6]1)(=[O:3])[CH3:2].C(Cl)(=O)C(Cl)=O.Cl.[NH2:42][CH2:43][C:44]([O:46][CH2:47][C:48]1[CH:53]=[CH:52][C:51]([N+:54]([O-:56])=[O:55])=[CH:50][CH:49]=1)=[O:45].CN1CCOCC1>ClCCl.CN(C)C=O>[C:1]([S:4][C@@H:5]1[CH2:9][N:8]([C:10]([O:12][CH2:13][C:14]2[CH:15]=[CH:16][C:17]([N+:20]([O-:22])=[O:21])=[CH:18][CH:19]=2)=[O:11])[C@H:7]([C:23](=[O:34])[NH:24][C:25]2[CH:30]=[CH:29][CH:28]=[C:27]([C:31]([NH:42][CH2:43][C:44]([O:46][CH2:47][C:48]3[CH:53]=[CH:52][C:51]([N+:54]([O-:56])=[O:55])=[CH:50][CH:49]=3)=[O:45])=[O:33])[CH:26]=2)[CH2:6]1)(=[O:3])[CH3:2]
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Komponenten

7

Edukt 4

HCID 79724-MethylmorpholineHCID 65578Oxalyl chloride2×HCID 22401149Glycine p-nitrobenzyl ester hydrochlorideHCID 57213936(2S,4S)-4-acetylthio-1-(4-nitrobenzyloxycarbonyl)-2-(3-carboxyphenylcarbamoyl)pyrrolidine

Produkt 1

HCID 57286643
(2S,4S)-4-acetylthio-1-(4-nitrobenzyloxycarbonyl)-2-(3-(4-nitrobenzyloxycarbonylmethylaminocarbonyl)phenylcarbamoyl)-pyrrolidine
Ausbeute 55,6 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6228DimethylformamideKatalysator2×HCID 6344DichloromethaneLösungsmittel4×

Versuchsvorschrift

To a solution of (2S,4S)-4-acetylthio-1-(4-nitrobenzyloxycarbonyl)-2-(3-carboxyphenylcarbamoyl)pyrrolidine (0.49 g, 1 mM) in dichloromethane (10 ml) was added oxalyl chloride (0.20 ml. 1.1 mM) and dimethylformamide (2-3 drops). After 1 hour a further amount of oxalyl chloride (0.20 ml, 1.1 mM) and DMF (2-3 drops) were added and the mixture stirred for a further hour. The solution was evaporated to leave a yellow gum. The gum was dissolved in dichloromethane (10 ml) and added to a suspension of 4-nitrobenzyl 2-aminoethanoate hydrochloride salt (0.30 g, 1.2 mM) and N-methylmorpholine (0.27 ml, 2.4 mM) in dichloromethane (10 ml). After 17 hours the mixture was diluted with dichloromethane (80 ml), washed with water (20 ml), brine (20 ml) and dried (MgSO4). Purification by flash chromatography through silica using a gradient of dichloromethane to ethyl acetate as eluent gave (2S,4S)-4-acetylthio-1-(4-nitrobenzyloxycarbonyl)-2-(3-(4-nitrobenzyloxycarbonylmethylaminocarbonyl)phenylcarbamoyl)-pyrrolidine (380 mg).

Aufarbeitung

  1. customThe solution was evaporated
  2. customto leave a yellow gum
  3. washwashed with water (20 ml), brine (20 ml)
  4. dry with materialdried (MgSO4)
  5. customPurification by flash chromatography through silica using a gradient of dichloromethane to ethyl acetate as eluent

Quellen und Nachweise

ORD-Eintrag
ord-65144a5d56fa4bf49870ae86bbac6abd
Quelldatensatz
uspto-grants-1996_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05527791

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