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4-Methylmorpholine → (+/-)-6-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-5-oxo-[1,4]diazepane-1-carboxylic acid ethyl ester

HRID 1890410
ノート
印刷プレビュー

反応式

HRID 1890410 の反応式
[NH2:1][CH2:2][CH2:3][N:4]([C:22]([O:24][CH2:25][CH3:26])=[O:23])[CH2:5][CH:6]([NH:10][C:11](=[O:21])[C:12]1[C:13](=[CH:17][CH:18]=[CH:19][CH:20]=1)[C:14]([OH:16])=O)[C:7](O)=[O:8].CN1CCOCC1.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=O)C=CC=CC=1>CN(C)C=O>[CH2:25]([O:24][C:22]([N:4]1[CH2:5][CH:6]([N:10]2[C:11](=[O:21])[C:12]3[C:13](=[CH:17][CH:18]=[CH:19][CH:20]=3)[C:14]2=[O:16])[C:7](=[O:8])[NH:1][CH2:2][CH2:3]1)=[O:23])[CH3:26]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 79724-MethylmorpholineHCID 199401P,P-Diphenylphosphinic azideHCID 66929928N-{2-[(2-amino-ethyl)-ethoxycarbonyl-amino]-1-carboxy-ethyl}-phthalamic acid

生成物 1

HCID 68735785(+/-)-6-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-5-oxo-[1,4]diazepane-1-carboxylic acid ethyl ester収率 33.4%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide
溶媒

実験手順

To a solution of 150.00 g (208.00 mmol) of N-{2-[(2-amino-ethyl)-ethoxycarbonyl-amino]-1-carboxy-ethyl}-phthalamic acid dissolved in 3 L of anhydrous dimethylformamide was added 75.50 mL (686.40 mmol) of N-methylmorpholine. The resulting mixture was stirred at room temperature for 10 min and 143.00 g (520.00 mmol) of diphenylphosphoryl azide was added. The mixture was stirred at room temperature for 36 h and evaporated to dryness. The mixture was dissolved in dichloromethane, washed with a saturated aqueous solution of ammonium chloride, saturated aqueous solution of sodium chloride, saturated aqueous solution of sodium hydrogen carbonate, dried over sodium sulfate and evaporated to dryness. The residue was chromatographed on silica gel eluting with a mixture of dichloromethane/methanol/aqueous ammonia solution (29%) in the proportions 96/4/0.6 led to afford 23.00 g (33%) of the desired compound.

後処理

  1. stirringThe mixture was stirred at room temperature for 36 h
  2. customevaporated to dryness
  3. dissolutionThe mixture was dissolved in dichloromethane
  4. washwashed with a saturated aqueous solution of ammonium chloride, saturated aqueous solution of sodium chloride, saturated aqueous solution of sodium hydrogen carbonate
  5. dry with materialdried over sodium sulfate
  6. customevaporated to dryness
  7. customThe residue was chromatographed on silica gel eluting with a mixture of dichloromethane/methanol/aqueous ammonia solution (29%) in the proportions 96/4/0.6

出典と根拠

ORDレコード
ord-224189a5197d4f26abd08c4f2e75da99
出典データセット
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08507476B2

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