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Dicyclohexylcarbodiimide → HCID 131711090、化合物

HRID 2083838
ノート
印刷プレビュー

反応式

HRID 2083838 の反応式
[CH3:1][O:2][C:3](=[O:53])[C@H:4]([CH2:49][CH:50]([CH3:52])[CH3:51])[NH:5][C:6](=[O:48])[C@@H:7]([CH2:41][C:42]1[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1)[NH:8][C:9](=[O:40])[C@H:10]([CH2:32][C:33]1[CH:38]=[CH:37][C:36]([OH:39])=[CH:35][CH:34]=1)[NH:11][C:12](=[O:31])[C@H:13]([CH2:29][OH:30])[NH:14][C:15](=[O:28])[C@H:16]([CH2:18][C:19]1[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[NH:21][CH:20]=1)[NH2:17].[CH3:54][O:55][C:56]1[CH:79]=[CH:78][C:59]([CH2:60][O:61][C:62]([NH:64][C@H:65]([C:75](O)=[O:76])[CH2:66][O:67][CH2:68][C:69]2[CH:74]=[CH:73][CH:72]=[CH:71][CH:70]=2)=[O:63])=[CH:58][CH:57]=1.ON1C2C=CC=CC=2N=N1.C1(N=C=NC2CCCCC2)CCCCC1>CN(C)C=O>[CH3:1][O:2][C:3](=[O:53])[C@H:4]([CH2:49][CH:50]([CH3:51])[CH3:52])[NH:5][C:6](=[O:48])[C@@H:7]([CH2:41][C:42]1[CH:43]=[CH:44][CH:45]=[CH:46][CH:47]=1)[NH:8][C:9](=[O:40])[C@H:10]([CH2:32][C:33]1[CH:38]=[CH:37][C:36]([OH:39])=[CH:35][CH:34]=1)[NH:11][C:12](=[O:31])[C@H:13]([CH2:29][OH:30])[NH:14][C:15](=[O:28])[C@H:16]([CH2:18][C:19]1[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[NH:21][CH:20]=1)[NH:17][C:75](=[O:76])[C@H:65]([CH2:66][O:67][CH2:68][C:69]1[CH:74]=[CH:73][CH:72]=[CH:71][CH:70]=1)[NH:64][C:62]([O:61][CH2:60][C:59]1[CH:78]=[CH:79][C:56]([O:55][CH3:54])=[CH:57][CH:58]=1)=[O:63]
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 10868DicyclohexylcarbodiimideHCID 757711-HydroxybenzotriazoleHCID 12764079HCID 12764079、化合物HCID 54560982HCID 54560982、化合物

生成物 1

HCID 131711090HCID 131711090、化合物

試薬・触媒・溶媒 1

HCID 6228
Dimethylformamide
溶媒

実験手順

L-Tryptophyl-L-seryl-L-tyrosyl-D-phenylalanyl-L-leucine methyl ester (example 1, h), 1.6 g., is dissolved in 30 ml. of dimethylformamide and treated with 0.789 g., of Nα -p-methoxybenzyloxycarbonyl-O-benzyl-L-serine and cooled in an ice bath. 1-Hydroxybenzotriazole, 326 mg., and finally 500 mg., of dicyclohexylcarbodiimide are added and the reaction mixture stirred to room temperature overnight and for twenty-four additional hours. The reaction mixture is filtered and the solvent removed under reduced pressure. The residue is dissolved in 200 ml. of ethyl acetate and washed with 0.25 N hydrochloric acid, saturated sodium chloride solution, 5% sodium bicarbonate solution, and finally, saturated sodium chloride solution. The ethyl acetate solution is refrigerated for several days and a gelatinous precipitate separated. After triturating with ether for two hours, the above named product is separated and dried, 1.7 g.

後処理

  1. dissolution, is dissolved in 30 ml
  2. filtrationThe reaction mixture is filtered
  3. customthe solvent removed under reduced pressure
  4. dissolutionThe residue is dissolved in 200 ml
  5. washof ethyl acetate and washed with 0.25 N hydrochloric acid, saturated sodium chloride solution, 5% sodium bicarbonate solution
  6. waitThe ethyl acetate solution is refrigerated for several days
  7. customa gelatinous precipitate separated
  8. customAfter triturating with ether for two hours
  9. customthe above named product is separated
  10. customdried

出典と根拠

ORDレコード
ord-eb14355f7bc949e190d6b0606657f50b
出典データセット
uspto-grants-1978_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04086219

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート