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Acetone → HCID 54104319、化合物

HRID 373345
ノート
印刷プレビュー

反応式

HRID 373345 の反応式
S1C2C=CC=CC=2N=C1S[S:11][C@H:12]1[N:15]([CH:16]([C:30]([CH3:32])=[CH2:31])[C:17]([O:19][CH2:20][C:21]2[CH:26]=[CH:25][C:24]([N+:27]([O-:29])=[O:28])=[CH:23][CH:22]=2)=[O:18])[C:14](=[O:33])[C@H:13]1[NH:34][C:35](=[O:44])[CH2:36][O:37][C:38]1[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=1.O.[C:46]1(C)[CH:51]=[CH:50][C:49]([S:52]([O-:54])=[O:53])=[CH:48][CH:47]=1.[Na+].[CH3:57]C(C)=O>O.[N+]([O-])([O-])=O.[Ag+]>[C:48]1([CH3:57])[C:49]([S:52]([S:11][C@H:12]2[N:15]([CH:16]([C:30]([CH3:32])=[CH2:31])[C:17]([O:19][CH2:20][C:21]3[CH:26]=[CH:25][C:24]([N+:27]([O-:29])=[O:28])=[CH:23][CH:22]=3)=[O:18])[C:14](=[O:33])[C@H:13]2[NH:34][C:35](=[O:44])[CH2:36][O:37][C:38]2[CH:39]=[CH:40][CH:41]=[CH:42][CH:43]=2)(=[O:53])=[O:54])=[CH:50][CH:51]=[CH:46][CH:47]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 180Acetone2 回HCID 12912424HCID 12912424、化合物HCID 23682957Sodium 4-methylbenzene-1-sulfinate hydrate

生成物 1

HCID 54104319HCID 54104319、化合物

試薬・触媒・溶媒 2

HCID 24470Silver Nitrate触媒HCID 962Water
溶媒
2 回

実験手順

A suspension of 4-nitrobenzyl 2-[(3R,4R)-4-[(benzothiazol-2-yl)dithio]-3-phenoxyacetamido-2-oxo-azetidin-1-yl]-3-methyl-3-butenoate (XVIIIc, 3.25 g, 0.005 mole) in acetone (90 mL) and water (10 mL) was treated at room temperature with silver nitrate (1.06 g, 0.00625 mole), followed by treatment with a solution of sodium p-toluenesulfinate hydrate (0.90 g, 0.050 mole) in acetone (70 mL)--water (10 mL). The slurry was stirred for 1 h at room temperature under darkness. It was then filtered through Celite, which was washed with acetone. The volume of the filterate was reduced in vacuo, and the product was extracted into ether (3×250 mL). The ether phase was dried over magnesium sulfate and concentrated. Flash chromatography (silica gel, 50% ethyl acetate in hexane) gave the pure title product, XVIIId, as a solid (2.053 g, 62%).

後処理

  1. filtrationIt was then filtered through Celite, which
  2. washwas washed with acetone
  3. extractionthe product was extracted into ether (3×250 mL)
  4. dry with materialThe ether phase was dried over magnesium sulfate
  5. concentrationconcentrated

出典と根拠

ORDレコード
ord-43346b19c54a4661aba9a2a50046f6cc
出典データセット
uspto-grants-1992_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05162521

反応ノート

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