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Tert-butyl 2-(butylamino)acetate → N2 (6,7-dimethoxy-2-naphthylsulfonly)-L-arginyl-N-butylglycine tert-butyl ester

HRID 1764701
ノート
印刷プレビュー

反応式

HRID 1764701 の反応式
[N:1]#[N:2].C(OC(=O)CN(C(=O)[C@H](CCCNC(=N)N)NS(C1C=CC2C(=CC(C)=C(C)C=2)C=1)(=O)=O)CCCC)(C)(C)C.[C:42]([O:46][C:47](=[O:54])[CH2:48][NH:49][CH2:50][CH2:51][CH2:52][CH3:53])([CH3:45])([CH3:44])[CH3:43].N#N.[CH3:57][O:58][C:59]1[CH:60]=[C:61]2[C:66](=[CH:67][C:68]=1[O:69][CH3:70])[CH:65]=[C:64]([S:71]([NH:74][C@H:75]([C:83](Cl)=[O:84])[CH2:76][CH2:77][CH2:78][NH:79][C:80](=[NH:82])[NH2:81])(=[O:73])=[O:72])[CH:63]=[CH:62]2>C(Cl)(Cl)Cl>[N:1]#[N:2].[C:42]([O:46][C:47](=[O:54])[CH2:48][N:49]([C:83](=[O:84])[C@H:75]([CH2:76][CH2:77][CH2:78][NH:79][C:80](=[NH:81])[NH2:82])[NH:74][S:71]([C:64]1[CH:63]=[CH:62][C:61]2[C:66](=[CH:67][C:68]([O:69][CH3:70])=[C:59]([O:58][CH3:57])[CH:60]=2)[CH:65]=1)(=[O:73])=[O:72])[CH2:50][CH2:51][CH2:52][CH3:53])([CH3:45])([CH3:44])[CH3:43]
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 22768716Tert-butyl 2-(butylamino)acetateHCID 178449150HCID 178449150、化合物HCID 178486633HCID 178486633、化合物

生成物 1

HCID 178449151N2 (6,7-dimethoxy-2-naphthylsulfonly)-L-arginyl-N-butylglycine tert-butyl ester収率 82%

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

N2 -(6,7-dimethyl-2-naphthylsulfonyl)-L-arginyl-N-butylglycine tert-butyl ester: To a stirred solution of 2.64 g of N-butylglycine tert-butyl ester in 20 ml of chloroform was carefully added N2 -(6,7-dimethoxy-2-naphthylsulfonyl)-L-arginyl chloride obtained above. The reaction mixture was allowed to stand at room temperature for one hour. At the end of this period, the reaction mixture was washed twice with 20 ml of saturated sodium chloride solution and evaporated to dryness. The residue was triturated with a small amount of water to give a crystalline material. This was collected by filtration and recrystallized from ethanol-ethyl ether to give 2.28 g (82 percent) of N2 -(6,7-dimethoxy-2-naphthylsulfonyl)-L-arginyl-N-butylglycine tert-butyl ester, M.P. 164°-166° C, I.R. (KBr): 3,390, 3,165, 1,735, 1,370 cm-1.

後処理

  1. customobtained above
  2. washAt the end of this period, the reaction mixture was washed twice with 20 ml of saturated sodium chloride solution
  3. customevaporated to dryness
  4. customThe residue was triturated with a small amount of water
  5. customto give a crystalline material
  6. filtrationThis was collected by filtration
  7. customrecrystallized from ethanol-ethyl ether

出典と根拠

ORDレコード
ord-17f1f4bd2d66418ebe34bb49b454d74d
出典データセット
uspto-grants-1978_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04117127

反応ノート

読み込み中…

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