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Dicyclohexylcarbodiimide → HCID 86735999、化合物

HRID 1763735
ノート
印刷プレビュー

反応式

HRID 1763735 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].[C:54]([O:58][C:59]([NH:61][C@H:62]([C:72]([OH:74])=O)[CH2:63][O:64][CH2:65][C:66]1[CH:71]=[CH:70][CH:69]=[CH:68][CH:67]=1)=[O:60])([CH3:57])(C)C.ON1[C:80]2C=CC=C[C:79]=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:72](=[O:74])[C@H:62]([CH2:63][O:64][CH2:65][C:66]1[CH:67]=[CH:68][CH:69]=[CH:70][CH:71]=1)[NH:61][C:59]([O:58][CH2:54][CH2:57][CH2:79][CH3:80])=[O:60]
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 90234L-Serine, N-[(1,1-dimethylethoxy)carbonyl]-O-(phenylmethyl)-HCID 54560982HCID 54560982、化合物

生成物 1

HCID 86735999HCID 86735999、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, 1.53 g., is dissolved in 35 ml. of dimethylformamide, the solution cooled in ice and treated with 620 mg. of Nα -t-butoxycarbonyl-O-benzyl-L-serine, 311 mg. of 1-hydroxybenztriazole and 475 mg. of dicyclohexylcarbodiimide (10% excess). The reaction is stirred overnight to room temperature and twenty-four hours additional at room temperature. The mixture is filtered and the filtrate evaporated under reduced pressure. The residue is dissolved in 500 ml. of ethyl acetate and washed with 0.1N hydrochloric acid, saturated salt solution, 5% sodium bicarbonate solution, saturated salt solution and water. The ethyl acetate solution is dried over magnesium sulfate and evaporated. The residual solid is dried under reduced pressure; 2.29 g.; m.p. 200°-202° C.; [α]D23 -19.5° (c 1.03, methanol); ultraviolet in methanol λmax 289.5 E11 52; λmax 280 E11 68.

後処理

  1. dissolution, is dissolved in 35 ml
  2. additiontreated with 620 mg
  3. filtrationThe mixture is filtered
  4. customthe filtrate evaporated under reduced pressure
  5. dissolutionThe residue is dissolved in 500 ml
  6. washof ethyl acetate and washed with 0.1N hydrochloric acid, saturated salt solution, 5% sodium bicarbonate solution, saturated salt solution and water
  7. dry with materialThe ethyl acetate solution is dried over magnesium sulfate
  8. customevaporated
  9. customThe residual solid is dried under reduced pressure

出典と根拠

ORDレコード
ord-b7d25f8b897145bfadb26f2390a8d3ba
出典データセット
uspto-grants-1978_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04111923

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