Ethyl Acetate → Allyl (1R,5S,6S)-6-((1R)-1-hydroxyethyl)-1-methyl-2-[[(Z)-2-(4-(N-4-nitrobenzyloxycarbonyl-L-valinyloxy-methyl)thiazol-5-yl)ethen-1-yl]thio]-1-carbapen-2-em-3-carboxylate

HRID 1799734ノート

反応式

HRID 1799734 の反応式
[OH:1][C@@H:2]([C@H:4]1[C:27](=[O:28])[N:6]2[C:7]([C:21]([O:23][CH2:24][CH:25]=[CH2:26])=[O:22])=[C:8]([S:11]/[CH:12]=[CH:13]\[C:14]3[S:18][CH:17]=[N:16][C:15]=3[CH2:19][OH:20])[C@H:9]([CH3:10])[C@H:5]12)[CH3:3].Cl.CN(C)CCCN=C=NCC.[N+:41]([C:44]1[CH:61]=[CH:60][C:47]([CH2:48][O:49][C:50]([NH:52][C@H:53]([C:57](O)=[O:58])[CH:54]([CH3:56])[CH3:55])=[O:51])=[CH:46][CH:45]=1)([O-:43])=[O:42].C(OCC)(=O)C>CN(C)C(=O)C.CN(C)C1C=CN=CC=1.[Cl-].[Na+].O>[OH:1][C@@H:2]([C@H:4]1[C:27](=[O:28])[N:6]2[C:7]([C:21]([O:23][CH2:24][CH:25]=[CH2:26])=[O:22])=[C:8]([S:11]/[CH:12]=[CH:13]\[C:14]3[S:18][CH:17]=[N:16][C:15]=3[CH2:19][O:20][C:57](=[O:58])[C@H:53]([CH:54]([CH3:55])[CH3:56])[NH:52][C:50]([O:49][CH2:48][C:47]3[CH:60]=[CH:61][C:44]([N+:41]([O-:43])=[O:42])=[CH:45][CH:46]=3)=[O:51])[C@H:9]([CH3:10])[C@H:5]12)[CH3:3]

参加物

8

反応物 4

HCID 8857Ethyl AcetateHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 54494215L-Valine, N-[[(4-nitrophenyl)methoxy]carbonyl]-HCID 69471839Allyl (1r,5s,6s)-6-((1r)-1-hydroxyethyl)-2-[[(z)-2-(4-hydroxymethylthiazol-5-yl)ethen-1-yl]thio]-1-methyl-1-carbapen-2-em-3-carboxylate

生成物 1

HCID 131728009Allyl (1R,5S,6S)-6-((1R)-1-hydroxyethyl)-1-methyl-2-[[(Z)-2-(4-(N-4-nitrobenzyloxycarbonyl-L-valinyloxy-methyl)thiazol-5-yl)ethen-1-yl]thio]-1-carbapen-2-em-3-carboxylate収率 32.1%

試薬・触媒・溶媒 3

HCID 142844-(Dimethylamino)pyridine触媒HCID 31374Dimethylacetamide溶媒HCID 57417360Sodium chloride; water溶媒

実験手順

Allyl (1R,5S,6S)-6-((1R)-1-hydroxyethyl)-2-[[(Z)-2-(4-hydroxymethylthiazol-5-yl)ethen-1-yl]thio]-1-methyl-1-carbapen-2-em-3-carboxylate (970 mg) was dissolved in 10 ml of N,N-dimethylacetamide. 4-Dimethylaminopyridine (281 mg), 441 mg of 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride, and 681 mg of N-4-nitrobenzyloxycarbonyl-L-valine were added to the solution, and the mixture was stirred at room temperature overnight. The reaction mixture was poured into 50 ml of 20% brine and 50 ml of ethyl acetate, followed by separation. The organic layer was dried over magnesium sulfate. The magnesium sulfate was removed by filtration, and the solvent was removed by distillation under the reduced pressure. The crude product was purified by column chromatography on silica gel (ethyl acetate:n-hexane=2:1, and subsequently ethyl acetate:n-hexane=5:1) to give 517 mg of allyl (1R,5S,6S)-6-((1R)-1-hydroxyethyl)-1-methyl-2-[[(Z)-2-(4-(N-4-nitrobenzyloxycarbonyl-L-valyloxymethyl)thiazol-5-yl)ethen-1-yl]thio]-1-carbapen-2-em-3-carboxylate.

後処理

  1. customfollowed by separation
  2. dry with materialThe organic layer was dried over magnesium sulfate
  3. customThe magnesium sulfate was removed by filtration
  4. customthe solvent was removed by distillation under the reduced pressure
  5. customThe crude product was purified by column chromatography on silica gel (ethyl acetate

出典と根拠

ORDレコード
ord-1c640564d51248afb91aaa3279a4f1e9
出典データセット
uspto-grants-2013_01
特許番号
US08344154B2

反応ノート

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