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Triphenylphosphine → Tert-butyl 2-(2-(benzyloxy)-5-(2-(pyrrolidin-1-yl)ethoxy)benzamido)-4-phenylbenzoate

HRID 454652
ノート
印刷プレビュー

反応式

HRID 454652 の反応式
[OH:1][CH2:2][CH2:3][N:4]1[CH2:8][CH2:7][CH2:6][CH2:5]1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N(C(OC(C)C)=O)=NC(OC(C)C)=O.[CH2:42]([O:49][C:50]1[CH:77]=[CH:76][C:75](O)=[CH:74][C:51]=1[C:52]([NH:54][C:55]1[CH:67]=[C:66]([C:68]2[CH:73]=[CH:72][CH:71]=[CH:70][CH:69]=2)[CH:65]=[CH:64][C:56]=1[C:57]([O:59][C:60]([CH3:63])([CH3:62])[CH3:61])=[O:58])=[O:53])[C:43]1[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=1>O1CCCC1>[CH2:42]([O:49][C:50]1[CH:77]=[CH:76][C:75]([O:1][CH2:2][CH2:3][N:4]2[CH2:8][CH2:7][CH2:6][CH2:5]2)=[CH:74][C:51]=1[C:52]([NH:54][C:55]1[CH:67]=[C:66]([C:68]2[CH:73]=[CH:72][CH:71]=[CH:70][CH:69]=2)[CH:65]=[CH:64][C:56]=1[C:57]([O:59][C:60]([CH3:63])([CH3:62])[CH3:61])=[O:58])=[O:53])[C:43]1[CH:44]=[CH:45][CH:46]=[CH:47][CH:48]=1
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 11776Triphenylphosphine4 回HCID 75555Diisopropyl diazene-1,2-dicarboxylate4 回HCID 762881-Pyrrolidineethanol4 回HCID 66990772Tert-butyl 2-(2-(benzyloxy)-5-hydroxybenzamido)-4-phenylbenzoate

生成物 1

HCID 66990790Tert-butyl 2-(2-(benzyloxy)-5-(2-(pyrrolidin-1-yl)ethoxy)benzamido)-4-phenylbenzoate

試薬・触媒・溶媒

1
HCID 8028Tetrahydrofuran溶媒

実験手順

1-(2-Hydroxyethyl)pyrrolidine (0.016 mL), triphenylphosphine (0.038 g), and diisopropyl azodicarboxylate (0.029 mL) were added to a tetrahydrofuran (1.2 mL) solution of tert-butyl 2-(2-(benzyloxy)-5-hydroxybenzamido)-4-phenylbenzoate (0.060 g), followed by stirring at room temperature for 25 minutes. To the reaction mixture, 1-(2-hydroxyethyl)pyrrolidine (0.016 mL), triphenylphosphine (0.038 g), and diisopropyl azodicarboxylate (0.029 mL) were added, followed by stirring at room temperature for 20 minutes. To the reaction mixture, 1-(2-hydroxyethyl)pyrrolidine (0.016 mL), triphenylphosphine (0.038 g), and diisopropyl azodicarboxylate (0.029 mL) were added, followed by stirring at room temperature for 30 minutes. To the reaction mixture, 1-(2-hydroxyethyl)pyrrolidine (0.016 mL), triphenylphosphine (0.038 g), and diisopropyl azodicarboxylate (0.029 mL) were added, followed by stirring at room temperature for 1 hour. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography [eluent: 80-0% hexane/ethyl acetate] to obtain 0.071 g of tert-butyl 2-(2-(benzyloxy)-5-(2-(pyrrolidin-1-yl)ethoxy)benzamido)-4-phenylbenzoate.

後処理

  1. stirringby stirring at room temperature for 20 minutes
  2. stirringby stirring at room temperature for 30 minutes
  3. stirringby stirring at room temperature for 1 hour
  4. customThe solvent was evaporated under reduced pressure
  5. customthe obtained residue was purified by silica gel column chromatography [eluent: 80-0% hexane/ethyl acetate]

出典と根拠

ORDレコード
ord-852726363910460985e4e90b0fe0e484
出典データセット
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08492582B2

反応ノート

読み込み中…

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