Di-p-tolylcarbodiimide → HCID 178426524、化合物

HRID 1813887ノート

反応式

HRID 1813887 の反応式
Cl.[CH2:2]([O:9][C:10](=[O:23])[C@H:11]([CH2:13][C:14]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[NH:16][CH:15]=1)N)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.C([N:27](C(C)C)CC)(C)C.[C:33]1([CH3:49])[CH:38]=[CH:37][C:36]([N:39]=[C:40]=[N:41][C:42]2[CH:47]=[CH:46][C:45]([CH3:48])=[CH:44][CH:43]=2)=[CH:35][CH:34]=1>CN(C=O)C>[C:33]1([CH3:49])[CH:38]=[CH:37][C:36]([N:39]([CH:11]([CH2:13][C:14]2[C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[NH:16][CH:15]=2)[C:10]([O:9][CH2:2][C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=2)=[O:23])[C:40]([NH:41][C:42]2[CH:43]=[CH:44][C:45]([CH3:48])=[CH:46][CH:47]=2)=[NH:27])=[CH:35][CH:34]=1

参加物

5

実験手順

1.0 mmol of tryptophan benzyl ester hydrochloride was dissolved in 20 ml of DMF and 1.1 mmol of diisopropylethylamine was added. After 10 min, 1.0 mmol of 1,3 di-p-tolylcarbodiimide was added to the stirred solution. The reaction mixture was stirred overnight in room temperature. The precipitated solid was filtered off and washed twice with 1 ml of DMF. To the collected filtrate, 50 ml of water was added. The precipitated solid was collected by filtration and washed with water. The solid was dissolved in ethyl acetate and 0.1 ml of conc. HCl was added. The pure product was precipitated from the solution with ethyl ether. Yield of pure compound=79%.

後処理

  1. filtrationThe precipitated solid was filtered off
  2. washwashed twice with 1 ml of DMF
  3. additionTo the collected filtrate, 50 ml of water was added
  4. filtrationThe precipitated solid was collected by filtration
  5. washwashed with water
  6. dissolutionThe solid was dissolved in ethyl acetate
  7. addition0.1 ml of conc. HCl was added
  8. customThe pure product was precipitated from the solution with ethyl ether

出典と根拠

ORDレコード
ord-f3d466c8f3b941adb6358af8846a5256
出典データセット
uspto-grants-2005_04
特許番号
US06875759B1

反応ノート

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