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Dichloromethane → HCID 178445899、化合物

HRID 1607413
ノート
印刷プレビュー

反応式

HRID 1607413 の反応式
[C:1]1([CH2:11][NH:12][C:13]([CH:15]([CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[C:16](O)=[O:17])=[O:14])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.C(N1C=CN=C1)(N1C=CN=C1)=O.ClCCl.[NH2:41][C@H:42]([C:49]([NH:51][C@H:52]([CH:57]=[N:58][NH:59][C:60]([NH2:62])=[O:61])[CH2:53][CH:54]([CH3:56])[CH3:55])=[O:50])[CH2:43][C:44]1[N:48]=[CH:47][NH:46][CH:45]=1>CN(C)C=O.C(N(CC)CC)C>[C:1]1([CH2:11][NH:12][C:13]([CH:15]([CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[C:16]([NH:41][C@H:42]([C:49]([NH:51][C@H:52]([CH:57]=[N:58][NH:59][C:60]([NH2:62])=[O:61])[CH2:53][CH:54]([CH3:56])[CH3:55])=[O:50])[CH2:43][C:44]2[N:48]=[CH:47][NH:46][CH:45]=2)=[O:17])=[O:14])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 6344DichloromethaneHCID 682631,1'-CarbonyldiimidazoleHCID 14600096(+/-)-2-(1-Naphthylmethylcarbamoyl)-3-phenylpropionic acidHCID 178445905HCID 178445905、化合物

生成物 1

HCID 178445899HCID 178445899、化合物収率 12.6%

試薬・触媒・溶媒 2

HCID 6228
Dimethylformamide
溶媒
HCID 8471Triethylamine溶媒

実験手順

A mixture of 102 mg of (±)-2-(1-naphthylmethylcarbamoyl)-3-phenylpropionic acid and 50 mg of 1,1'-carbonyldiimidazole was added to 5 ml of dichloromethane, and the mixture was stirred for 40 minutes at room temperature. The reaction mixture was added to a solution of 202 mg of L-histidyl-L-leucinal semicarbazone.2p-toluenesulfonic acid salt and 0.09 ml of triethylamine in 3 ml of N,N-dimethylformamide, and the mixture was stirred overnight at room temperature. The reaction mixture was concentrated under reduced pressure, and a 5% aqueous sodium bicarbonate solution was added to the residue. The mixture was extracted with ethyl acetate, dried and concentrated under reduced pressure. The residue was purified by preparative silica gel thin layer chromatography (developing solvent: lower layer of chloroform/methanol/water=8/3/1 by volume) to obtain 24 mg of N-[(±)-2-(1-naphthylmethylcarbamoyl)-3-phenylpropionyl]-L-histidyl-L-leucinal semicarbazone as a white powder.

後処理

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. additiona 5% aqueous sodium bicarbonate solution was added to the residue
  3. extractionThe mixture was extracted with ethyl acetate
  4. customdried
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by preparative silica gel thin layer chromatography (developing solvent: lower layer of chloroform/methanol/water=8/3/1 by volume)

出典と根拠

ORDレコード
ord-78f84b598104434f95eb0143dd5f708c
出典データセット
uspto-grants-1989_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04863904

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