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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Methanol → HCID 131736690、化合物

HRID 1482249
ノート
印刷プレビュー

反応式

HRID 1482249 の反応式
[CH:1]1[CH:6]=[CH:5][C:4]([C:7]([Cl:21])([C:14]2[C:19]([Cl:20])=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[CH:3][CH:2]=1.CO.C(N(C(C)C)CC)(C)C.[CH:33]1[C:45]2[CH:44]([CH2:46][O:47][C:48]([NH:50][C@H:51]([C:67](=[O:74])[N:68]3[CH2:73][CH2:72][CH2:71][CH2:70][CH2:69]3)[CH2:52][C:53]3[CH:58]=[CH:57][C:56]([CH2:59][CH2:60][CH2:61][CH2:62][CH2:63][C:64]([OH:66])=[O:65])=[CH:55][CH:54]=3)=[O:49])[C:43]3[C:38](=[CH:39][CH:40]=[CH:41][CH:42]=3)[C:37]=2[CH:36]=[CH:35][CH:34]=1>ClCCl>[CH:42]1[C:43]2[CH:44]([CH2:46][O:47][C:48]([NH:50][C@H:51]([C:67](=[O:74])[N:68]3[CH2:69][CH2:70][CH2:71][CH2:72][CH2:73]3)[CH2:52][C:53]3[CH:54]=[CH:55][C:56]([CH2:59][CH2:60][CH2:61][CH2:62][CH2:63][C:64]([OH:66])=[O:65])=[CH:57][CH:58]=3)=[O:49])[C:45]3[C:37](=[CH:36][CH:35]=[CH:34][CH:33]=3)[C:38]=2[CH:39]=[CH:40][CH:41]=1.[CH:11]1[CH:10]=[CH:9][C:8]([C:7]([Cl:21])([C:14]2[C:19]([Cl:20])=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:4]2[CH:5]=[CH:6][CH:1]=[CH:2][CH:3]=2)=[CH:13][CH:12]=1
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 887MethanolHCID 81531DiisopropylethylamineHCID 945242-Chlorotrityl chlorideHCID 89668315HCID 89668315、化合物

生成物 1

HCID 131736690HCID 131736690、化合物収率 223.2%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane
溶媒
2 回

実験手順

2-Chlorotrityl chloride resin (1.07 mmol/g, 100-200 mesh, 1% DVB, manufactured by Chem-Impex, 3.00 g, 3.21 mmol) and dichloromethane (20 ml) were mixed, followed by shaking at room temperature. Dichloromethane was removed, after which methanol (0.52 ml, 12.85 mmol) and diisopropylethylamine (1.35 ml, 7.75 mmol) were added to a solution of (S)-6-(4-(2-((((9H-fluoren-9-yl)methoxy) carbonyl)amino)-3-oxo-3-(piperidin-1-yl)propyl)phenyl)hexanoic acid (Compound SP427) (0.91 g, 1.60 mmol) in dichloromethane (14 ml) and the resulting mixture was added to the resin, followed by shaking at room temperature for 5 minutes. The reaction solution was removed, after which methanol (4.2 ml) and diisopropylethylamine (1.4 ml) were added to dichloromethane (14 ml), and the resulting mixture was added, followed by shaking at room temperature for 2.5 hours. This reaction solution was removed, and dichloromethane (20 ml) was then placed, followed by shaking. Dichloromethane was removed, and dichloromethane (20 ml) was then placed again, followed by shaking. Dichloromethane was removed, and the resin was then dried under reduced pressure to afford the title compound (Compound SP428) (3.15 g).

後処理

  1. customDichloromethane was removed
  2. additionthe resulting mixture was added to the resin
  3. stirringby shaking at room temperature for 5 minutes
  4. customThe reaction solution was removed
  5. additionafter which methanol (4.2 ml) and diisopropylethylamine (1.4 ml) were added to dichloromethane (14 ml)
  6. additionthe resulting mixture was added
  7. stirringby shaking at room temperature for 2.5 hours
  8. customThis reaction solution was removed
  9. stirringby shaking
  10. customDichloromethane was removed
  11. stirringby shaking
  12. customDichloromethane was removed
  13. customthe resin was then dried under reduced pressure

出典と根拠

ORDレコード
ord-9f89edc86b9e4e9d8e21caac17d34345
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09409952B2

反応ノート

読み込み中…

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