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Triphenylphosphine → Allyl (1S,5R,6S)-1-methyl-2-(1,1-dioxo-2,5,6,7-tetrahydro-1-thia-2,6-diaza-cyclopenta[cd]phenalen-2-ylmethyl)-6-(1-(R)-allyloxycarbonyloxyethyl)-carbapen-2-em-3-carboxylate

HRID 1068564
ノート
印刷プレビュー

反応式

HRID 1068564 の反応式
CCOC(/N=N/C(OCC)=O)=O.O[CH2:14][C:15]1[C@H:16]([CH3:38])[C@@H:17]2[C@@H:27]([C@H:28]([O:30][C:31]([O:33][CH2:34][CH:35]=[CH2:36])=[O:32])[CH3:29])[C:26](=[O:37])[N:18]2[C:19]=1[C:20]([O:22][CH2:23][CH:24]=[CH2:25])=[O:21].[S:39]1(=[O:55])(=[O:54])[C:43]2[CH:44]=[CH:45][C:46]3[CH2:47][NH:48][CH2:49][C:50]4[C:53]=3[C:42]=2[C:41](=[CH:52][CH:51]=4)[NH:40]1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>O1CCCC1>[CH3:38][C@@H:16]1[C@@H:17]2[C@@H:27]([C@H:28]([O:30][C:31]([O:33][CH2:34][CH:35]=[CH2:36])=[O:32])[CH3:29])[C:26](=[O:37])[N:18]2[C:19]([C:20]([O:22][CH2:23][CH:24]=[CH2:25])=[O:21])=[C:15]1[CH2:14][N:40]1[C:41]2[C:42]3[C:53]4[C:50](=[CH:51][CH:52]=2)[CH2:49][NH:48][CH2:47][C:46]=4[CH:45]=[CH:44][C:43]=3[S:39]1(=[O:55])=[O:54]
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 4

HCID 11776TriphenylphosphineHCID 5462977Diethyl azodicarboxylateHCID 11046746allyl (1S,5R,6S)-2-(hydroxymethyl)-6-[1(R)-allyloxycarbonyloxy-ethyl]-1-methylcarbapen-2-em-3-carboxylateHCID 206661122,5,6,7-Tetrahydro-1-thia-2,6-diaza-cyclopenta[cd]phenalene 1,1-dioxide

生成物 1

HCID 131722705
Allyl (1S,5R,6S)-1-methyl-2-(1,1-dioxo-2,5,6,7-tetrahydro-1-thia-2,6-diaza-cyclopenta[cd]phenalen-2-ylmethyl)-6-(1-(R)-allyloxycarbonyloxyethyl)-carbapen-2-em-3-carboxylate

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

Diethylazodicarboxylate (2.25 mmol) is added to a cold (0° C.) solution of allyl (1S,5R,6S)-2-(hydroxymethyl)-6-[1(R)-allyloxycarbonyloxy-ethyl]-1-methylcarbapen-2-em-3-carboxylate (1.5 mmol), 2,5,6,7-tetrahydro-1-thia-2,6-diaza-cyclopenta[cd]phenalene-1,1-dioxide (1.5 mmol) and triphenylphosphine (2.25 mmol) in tetrahydrofuran (15 mL). The mixture is stirred at room temperature for 30 minutes then partitioned between ethyl acetate (100 mL) and water (100 mL). The water layer is extracted with ethyl acetate (50 mL) and the combined ethyl acetate layers are washed with saturated aqueous sodium chloride (50 mL), dried with magnesium sulfate, filtered, and evaporated. The crude product is purified by column chromatography to give the title compound.

後処理

  1. customthen partitioned between ethyl acetate (100 mL) and water (100 mL)
  2. extractionThe water layer is extracted with ethyl acetate (50 mL)
  3. washthe combined ethyl acetate layers are washed with saturated aqueous sodium chloride (50 mL)
  4. dry with materialdried with magnesium sulfate
  5. filtrationfiltered
  6. customevaporated
  7. customThe crude product is purified by column chromatography

出典と根拠

ORDレコード
ord-672c6f05ad994ee8ad243315865d3d4d
出典データセット
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06251890B1

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート