ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Ethyl Acetate → pivaloyloxymethyl 7-[2-(Boc-L-alanyl)aminothiazol-4-yl]-2-methoxyimino-3-cephem-4-carboxylate

HRID 274242
ノート
印刷プレビュー

反応式

HRID 274242 の反応式
P(Cl)(Cl)(Cl)=O.[C:6]([NH:13][C@H:14]([C:16]([NH:18][C:19]1[S:20][CH:21]=[C:22]([C:24](=NOC)[C:25]([OH:27])=O)[N:23]=1)=[O:17])[CH3:15])([O:8][C:9]([CH3:12])([CH3:11])[CH3:10])=[O:7].NC1C(=O)[N:34]2[C:35]([C:39]([O:41][CH2:42][O:43][C:44](=[O:49])[C:45]([CH3:48])([CH3:47])[CH3:46])=[O:40])=[CH:36][CH2:37][S:38][C@H:33]12.C[Si](C)(C)[NH:54]C(=O)C.C([O:63][CH2:64]C)(=O)C>C(Cl)Cl.CN(C=O)C>[C:6]([NH:13][C@H:14]([C:16]([NH:18][C:19]1[S:20][CH:21]=[C:22]([CH:24]2[C:25](=[O:27])[N:34]3[C:35]([C:39]([O:41][CH2:42][O:43][C:44](=[O:49])[C:45]([CH3:46])([CH3:47])[CH3:48])=[O:40])=[CH:36][C:37](=[N:54][O:63][CH3:64])[S:38][C@H:33]23)[N:23]=1)=[O:17])[CH3:15])([O:8][C:9]([CH3:10])([CH3:11])[CH3:12])=[O:7]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 8857Ethyl Acetate2 回HCID 24813Phosphorus oxychlorideHCID 25989Acetamide, N-(trimethylsilyl)-HCID 538373702-[2-(Boc-L-alanyl)aminothiazol-4-yl]-2-methoxyiminoacetic acidHCID 67719473Pivaloyloxymethyl 7-amino-3-cephem-4-carboxylate

生成物 1

HCID 131718849
pivaloyloxymethyl 7-[2-(Boc-L-alanyl)aminothiazol-4-yl]-2-methoxyimino-3-cephem-4-carboxylate

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 6344Dichloromethane溶媒2 回

反応条件

温度
-10 °C

実験手順

A mixture of dry ethyl acetate (1.82 ml) and dry DMF (0.36 ml) was cooled to --10° C. Phosphorus oxychloride (0.37 ml) was added thereto, and the mixture was stirred at said temperature for 20 minutes. A solution of the compound of Example 1 (1.35 g) in dry methylene chloride (8.0 ml) was added thereto, and the mixture was stirred at a temperature between -10° to -5° C. for 30 minutes. On the other hand, pivaloyloxymethyl 7-amino-3-cephem-4-carboxylate (0.95 g) was dissolved in dry methylene chloride (12 ml), and N-trimethylsilylacetamide (0.79 g) was added thereto, and the mixture was cooled to -15° C. Thereto was dropwise added the aforementioned solution, and the mixture was stirred at said temperature for 45 minutes. Ethyl acetate (200 ml) was added thereto, and the mixture was washed with 5% aqueous solution of sodium bicarbonate (100 ml) and saturated brine (100 ml). After drying over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The residue was subjected to silica gel column chromatography eluted with benzene-ethyl acetate. The object fraction was concentrated to give 1.32 g of pivaloyloxymethyl 7-[2-(Boc-L-alanyl)aminothiazol-4-yl]-2-methoxyimino-3-cephem-4-carboxylate (synisomer).

後処理

  1. customfor 20 minutes
  2. stirringthe mixture was stirred at a temperature between -10° to -5° C. for 30 minutes
  3. temperaturethe mixture was cooled to -15° C
  4. additionThereto was dropwise added the aforementioned solution
  5. stirringthe mixture was stirred
  6. customfor 45 minutes
  7. washthe mixture was washed with 5% aqueous solution of sodium bicarbonate (100 ml) and saturated brine (100 ml)
  8. dry with materialAfter drying over anhydrous sodium sulfate
  9. distillationthe solvent was distilled off under reduced pressure
  10. washeluted with benzene-ethyl acetate
  11. concentrationThe object fraction was concentrated

出典と根拠

ORDレコード
ord-9f5ca87869534a8cb894dd3eeb01cb1a
出典データセット
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05389625

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート