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Water → N-{2-[(2-amino-ethyl)-ethoxycarbonyl-amino]-1-carboxy-ethyl}-phthalamic acid

HRID 1890409
ノート
印刷プレビュー

反応式

HRID 1890409 の反応式
CO[C:3](=O)[CH:4]([N:22]1[C:30](=[O:31])[C:29]2[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=2)[C:23]1=[O:32])[CH2:5][N:6]([CH2:12][CH2:13][NH:14]C(OC(C)(C)C)=O)[C:7]([O:9][CH2:10][CH3:11])=[O:8].[OH2:34].[OH2:35].[OH-:36].[Li+]>O1CCCC1>[NH2:14][CH2:13][CH2:12][N:6]([C:7]([O:9][CH2:10][CH3:11])=[O:8])[CH2:5][CH:4]([NH:22][C:23](=[O:32])[C:24]1[C:29](=[CH:28][CH:27]=[CH:26][CH:25]=1)[C:30]([OH:31])=[O:36])[C:3]([OH:35])=[O:34]
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

5

反応物 3

HCID 962WaterHCID 168937Lithium hydroxide, monohydrate2 回HCID 669299233-[(2-Tert-butoxycarbonylamino-ethyl)-ethoxycarbonyl-amino]-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propionic acid methyl ester

生成物 1

HCID 66929928N-{2-[(2-amino-ethyl)-ethoxycarbonyl-amino]-1-carboxy-ethyl}-phthalamic acid

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran
溶媒

反応条件

温度
65 °C

実験手順

To a solution of 218.80 g (470.35 mmol) of 3-[(2-tert-butoxycarbonylamino-ethyl)-ethoxycarbonyl-amino]-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propionic acid methyl ester dissolved in 600 mL of tetrahydrofuran was added 100 mL of water and 39.47 g (940.70 mmol) of lithium hydroxide monohydrate. The resulting mixture was heated at 65° C. for 2 h. 19.73 g (470.35 mmol) of lithium hydroxide monohydrate was added. The resulting mixture was stirred at 65° C. for 1 h. The mixture was evaporated to dryness. Toluene was added to the residue and evaporated to dryness to give 225.00 g of the desired compound as a lithium salt. To the resulting lithium salt (225.00 g) suspension in 1 L of dichloromethane was added slowly 500 mL of trifluoroacetic acid. The resulting mixture was stirred at room temperature for 2 h30 and evaporated to dryness. The residue was triturated with a mixture of diethyl ether/dichloromethane and filtered to afford 300.00 g (89%) of a powder. The compound was used as such in the next step.

後処理

  1. customThe mixture was evaporated to dryness
  2. additionToluene was added to the residue
  3. customevaporated to dryness

出典と根拠

ORDレコード
ord-f069f803dffa4f499e66b9680141ddcd
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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