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p-Toluenesulfonic acid → HCID 178427522、化合物

HRID 652369
ノート
印刷プレビュー

反応式

HRID 652369 の反応式
[NH:1]([C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[C@H:2]([C:10]([OH:12])=O)[CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[NH2:20][C@H:21]([C:29]([O:31][CH2:32][C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)=[O:30])[CH2:22][CH2:23][CH2:24][NH:25][C:26](=[NH:28])[NH2:27].[S:39](O)([C:42]1[CH:48]=[CH:47][C:45]([CH3:46])=[CH:44][CH:43]=1)(=[O:41])=[O:40].C1C=CC2N(O)N=NC=2C=1>CN(C=O)C.CCCCCC.C(OCC)(=O)C>[NH:1]([C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[C@H:2]([C:10]([NH:20][C@H:21]([C:29]([O:31][CH2:32][C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)=[O:30])[CH2:22][CH2:23][CH2:24][NH:25][C:26](=[NH:27])[NH:28][S:39]([C:42]1[CH:48]=[CH:47][C:45]([CH3:46])=[CH:44][CH:43]=1)(=[O:41])=[O:40])=[O:12])[CH2:3][C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 6101p-Toluenesulfonic acidHCID 757711-HydroxybenzotriazoleHCID 77857L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-HCID 178512913HCID 178512913、化合物

生成物 1

HCID 178427522HCID 178427522、化合物

試薬・触媒・溶媒 3

HCID 6228Dimethylformamide
溶媒
HCID 8058Hexane溶媒
HCID 8857Ethyl Acetate溶媒2 回

実験手順

Boc-Phe-OH (4 g, 15 mmole), H-Arg-OBzl.TosOH (8.9 g, 15 mmole) and HOBt (2.1 g, 15.75 mmole) were dissolved in DMF (25 ml), and WSCI (12.9 ml, 15.75 mmole) was added dropwise thereto while cooling, and the thus-obtained mixture (pH=4) was stirred overnight. To the reaction solution, AcOEt (300 ml) was added thereto, and the solution was washed with 1N HCl, water and 5% NaHCO3 and water, in order, and dried with Na2SO4 . AcOEt was distilled off under reduced pressure, and the thus-obtained residue was treated with ethyl acetate, ether, and n-hexane to give an oily substance. The substance was obtained by decantation and treated with ethyl acetate and hexane to give precipitates of the object product (6.89 g, 60%).

後処理

  1. additionWSCI (12.9 ml, 15.75 mmole) was added dropwise
  2. temperaturewhile cooling
  3. washthe solution was washed with 1N HCl, water and 5% NaHCO3 and water, in order
  4. dry with materialdried with Na2SO4
  5. distillationAcOEt was distilled off under reduced pressure
  6. additionthe thus-obtained residue was treated with ethyl acetate, ether, and n-hexane
  7. customto give an oily substance
  8. customThe substance was obtained by decantation
  9. customto give
  10. customprecipitates of the object product (6.89 g, 60%)

出典と根拠

ORDレコード
ord-33c46450a8d148c4a62aa1d1f8fbf767
出典データセット
uspto-grants-1987_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04670540

反応ノート

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