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Sodium Hydroxide → HCID 68834969、化合物

HRID 747762
ノート
印刷プレビュー

反応式

HRID 747762 の反応式
[C:1]1([S:7]([NH:10][C@@H:11]([CH2:16][C:17]2[CH:22]=[CH:21][C:20]([O:23][CH:24]3[CH2:29][CH2:28][N:27]([C:30]([O:32][CH2:33][C:34]4[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=4)=[O:31])[CH2:26][CH2:25]3)=[CH:19][CH:18]=2)[C:12]([O:14]C)=O)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-].[Na+].Cl.Cl.[NH2:44][C:45]1[CH:46]=[C:47]([CH:51]=[CH:52][CH:53]=1)[C:48]([NH2:50])=[NH:49].CCN=C=NCCCN(C)C>CO.O1CCCC1.N1C=CC=CC=1>[C:48]([C:47]1[CH:46]=[C:45]([NH:44][C:12](=[O:14])[C@@H:11]([NH:10][S:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)(=[O:9])=[O:8])[CH2:16][C:17]2[CH:18]=[CH:19][C:20]([O:23][CH:24]3[CH2:29][CH2:28][N:27]([C:30]([O:32][CH2:33][C:34]4[CH:35]=[CH:36][CH:37]=[CH:38][CH:39]=4)=[O:31])[CH2:26][CH2:25]3)=[CH:21][CH:22]=2)[CH:53]=[CH:52][CH:51]=1)(=[NH:49])[NH2:50]
参加物反応条件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 14798Sodium HydroxideHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 3084651m-Aminobenzamidine dihydrochlorideHCID 86760713HCID 86760713、化合物

生成物 1

HCID 68834969HCID 68834969、化合物

試薬・触媒・溶媒 3

HCID 887Methanol
溶媒
HCID 1049Pyridine溶媒
HCID 8028Tetrahydrofuran溶媒

反応条件

温度
50 °C

実験手順

1.75 g (3.26 mmol) of methyl (2S)-2-(benzenesulfonylamino)-3-[4-[1-(benzyloxycarbonyl)-4-piperidyloxy]phenyl]propionate was dissolved in a mixed solvent of 10 ml of methanol and 10 ml of tetrahydrofuran. 6.52 ml (6.52 mmol) of 1 N aqueous sodium hydroxide solution was added to the solution, and they were stirred at 50° C. overnight. The reaction mixture was washed with ether and then made acidic with concentrated hydrochloric acid. After the isolation process with dichloromethane as the extractant in the same manner as that of step 1 in Example 1, an oily residue was obtained, which was dissolved in 60 ml of pyridine. 747 mg (3.61 mmol) of 3-aminobenzamidine dihydrochloride and 750 mg (3.92 mmol) of WSC were added to the solution, and they were stirred at room temperature overnight. The solvent was distilled off, and the residue was purified by the silica gel column chromatography to obtain the title compound.

後処理

  1. washThe reaction mixture was washed with ether
  2. customAfter the isolation process with dichloromethane as the extractant in the same manner as that of step 1 in Example 1, an oily residue was obtained
  3. stirringwere stirred at room temperature overnight
  4. distillationThe solvent was distilled off
  5. customthe residue was purified by the silica gel column chromatography

出典と根拠

ORDレコード
ord-6bb77e3980b54f5da2b29454cb94931d
出典データセット
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07396844B1

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート