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Diisopropylethylamine → (S)-1-(tert-Butyloxycarbonyl)-4-(dipentylcarbamoyl)piperazine-2-carboxylic acid

HRID 2226614
ノート
印刷プレビュー

反応式

HRID 2226614 の反応式
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][NH:11][CH2:10][C@H:9]1[C:14]([OH:16])=[O:15])=[O:7])([CH3:4])([CH3:3])[CH3:2].C(N(C(C)C)CC)(C)C.[CH2:26]([N:31]([CH2:35][CH2:36][CH2:37][CH2:38][CH3:39])[C:32](Cl)=[O:33])[CH2:27][CH2:28][CH2:29][CH3:30]>CN(C=O)C>[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][N:11]([C:32](=[O:33])[N:31]([CH2:35][CH2:36][CH2:37][CH2:38][CH3:39])[CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])[CH2:10][C@H:9]1[C:14]([OH:16])=[O:15])=[O:7])([CH3:4])([CH3:2])[CH3:3]
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 81531DiisopropylethylamineHCID 22106956Dipentylcarbamyl chlorideHCID 40419053(2S)-1-[(tert-butoxy)carbonyl]piperazine-2-carboxylic acid

生成物 1

HCID 53820654(S)-1-(tert-Butyloxycarbonyl)-4-(dipentylcarbamoyl)piperazine-2-carboxylic acid

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒2 回

実験手順

A partial solution of 1.32 g (5.74 mmole) of (S)-1-(tert-butyloxycarbonyl)piperazine-2-carboxylic acid in 25 ml of dried DMF was treated dropwise over 5 min with 1.48 g (11.47 mmole of diisopropylethyl amine at 25° under nitrogen with stirring. The clear solution which resulted was treated dropwise over 15 min with a solution of 1.26 g (5.74 mmole) of dipentylcarbamoyl chloride in 5 ml of DMF and the mixture was stirred under nitrogen at 25° for 16 hr. The solution was concentrated in vacuo and the residue was dissolved in 100 ml of dichloromethane which was extracted with 2×100 ml of 0.5M citric acid and 2×25 ml of water. Without drying, the solution was concentrated in vacuo to 1.85g (78%) of medium yellow oil which was homogeneous by the (silica gel, 1:1:1:1 ethylacetate: n-butanol: acetic acid: water, Rf =0.50).

後処理

  1. customThe clear solution which resulted
  2. stirringthe mixture was stirred under nitrogen at 25° for 16 hr
  3. concentrationThe solution was concentrated in vacuo
  4. dissolutionthe residue was dissolved in 100 ml of dichloromethane which
  5. extractionwas extracted with 2×100 ml of 0.5M citric acid and 2×25 ml of water
  6. customWithout drying
  7. concentrationthe solution was concentrated in vacuo to 1.85g (78%) of medium yellow oil which

出典と根拠

ORDレコード
ord-699c6f02937442eda9dbc481a36c069f
出典データセット
uspto-grants-1994_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05348955

反応ノート

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