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Dichloromethane → 3-(2-Tert-butoxycarbonylamino-ethylamino)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propionic acid methyl ester

HRID 1890407
ノート
印刷プレビュー

反応式

HRID 1890407 の反応式
[CH3:1][O:2][C:3](=[O:17])[C:4]([N:6]1[C:14](=[O:15])[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[C:7]1=[O:16])=[CH2:5].C(=O)([O-])[O-].[K+].[K+].[C:24]([O:28][C:29](=[O:34])[NH:30][CH2:31][CH2:32][NH2:33])([CH3:27])([CH3:26])[CH3:25].ClCCl>C(#N)C>[CH3:1][O:2][C:3](=[O:17])[CH:4]([N:6]1[C:14](=[O:15])[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[C:7]1=[O:16])[CH2:5][NH:33][CH2:32][CH2:31][NH:30][C:29]([O:28][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:34]
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 6344DichloromethaneHCID 11430Potassium CarbonateHCID 187201N-BOC-ethylenediamineHCID 599143Methyl 2-(1,3-dioxoisoindol-2-yl)prop-2-enoate

生成物 1

HCID 669298353-(2-Tert-butoxycarbonylamino-ethylamino)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propionic acid methyl ester収率 32.3%

試薬・触媒・溶媒 1

HCID 6342
Acetonitrile
溶媒

実験手順

To a solution of 12.60 g (51.38 mmol) of 2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-acrylic acid methyl ester (described in Synthetic Communications, 33(8), 1375-1382; 2003) dissolved in 170 mL of acetonitrile was added at room temperature 42.60 g (308.28 mmol) of potassium carbonate and 9.05 g (56.52 mmol) of (2-amino-ethyl)-carbamic acid tert-butyl ester. The resulting mixture was stirred at room temperature for 12 h. 300 mL of dichloromethane was added and the mixture was filtered and the solid obtained was triturated with dichloromethane, filtered, and the resulting filtrates were evaporated to dryness. The residue was dissolved in diethyl ether, washed with a saturated aqueous solution of sodium hydrogen carbonate, saturated aqueous solution of sodium chloride, dried over sodium sulfate and evaporated to dryness. The residue was chromatographed on silica gel eluting with a mixture of chloroform/methanol/aqueous ammonia solution (29%) in the proportions 98/2/0.2 led to afford 6.50 g (31%) of the desired compound.

後処理

  1. filtrationthe mixture was filtered
  2. customthe solid obtained
  3. customwas triturated with dichloromethane
  4. filtrationfiltered
  5. customthe resulting filtrates were evaporated to dryness
  6. dissolutionThe residue was dissolved in diethyl ether
  7. washwashed with a saturated aqueous solution of sodium hydrogen carbonate, saturated aqueous solution of sodium chloride
  8. dry with materialdried over sodium sulfate
  9. customevaporated to dryness
  10. customThe residue was chromatographed on silica gel eluting with a mixture of chloroform/methanol/aqueous ammonia solution (29%) in the proportions 98/2/0.2

出典と根拠

ORDレコード
ord-23fd94016b3f43a381aa43faacdc8027
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

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