ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
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
  1. ホーム
  2. /反応

Acetic Acid → N2 Isobutyryl-9-(3', 5'-di-O-[tetrahydropyran-2-yl]-beta-D-arabinofuranosyl)guanine

HRID 443325
ノート
印刷プレビュー

反応式

HRID 443325 の反応式
[N:1]#[N:2].[C:3]([NH:8][C:9]1[NH:10][C:11](=[O:44])[C:12]2[N:13]=[CH:14][N:15]([C@@H:18]3[O:30][C@H:29]([CH2:31][O:32][C:33]4(C(=O)C(C)C)[CH2:38][CH2:37][CH2:36][CH2:35][O:34]4)[C@@H:21]([O:22][CH:23]4[CH2:28][CH2:27][CH2:26][CH2:25][O:24]4)[C@@H:19]3[OH:20])[C:16]=2[N:17]=1)(=[O:7])[CH:4]([CH3:6])[CH3:5].[OH-].[Na+].C(O)(=O)C.C([O-])(O)=O.[Na+]>N1C=CC=CC=1.CO.O.CCO.CO>[N:1]#[N:2].[C:3]([NH:8][C:9]1[NH:10][C:11](=[O:44])[C:12]2[N:13]=[CH:14][N:15]([C@@H:18]3[O:30][C@H:29]([CH2:31][O:32][CH:33]4[CH2:38][CH2:37][CH2:36][CH2:35][O:34]4)[C@@H:21]([O:22][CH:23]4[CH2:28][CH2:27][CH2:26][CH2:25][O:24]4)[C@@H:19]3[OH:20])[C:16]=2[N:17]=1)(=[O:7])[CH:4]([CH3:6])[CH3:5]
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

7

反応物 4

HCID 176Acetic AcidHCID 14798Sodium HydroxideHCID 516892Sodium BicarbonateHCID 137231692N2 Isobutyryl-9-(2'-isobutyryl-3', 5'-di-O-[tetrahydropyran-2-yl]-beta-D-arabinofuranosyl) guanine

生成物 1

HCID 137231691N2 Isobutyryl-9-(3', 5'-di-O-[tetrahydropyran-2-yl]-beta-D-arabinofuranosyl)guanine収率 78.3%

試薬・触媒・溶媒

2
HCID 18681192Ethanol, mixt. with methanol溶媒HCID 21976680Pyridine methanol water溶媒

反応条件

温度
0 °C

実験手順

N2 -Isobutyryl-9-(2'-isobutyryl-3', 5'-di-O-[tetrahydropyran-2-yl]-β-D-arabinofuranosyl) guanine (5.58 g) was dissolved in pyridine-MeOH-H2O (65:30:15, 52 mL) at room temperature. The solution was cooled to 0° C. and 52 mL of 2 N NaOH in EtOH-MeOH (95:5) was added slowly, followed by stirring for 2 hours at 0° C. Glacial acetic acid was added to pH 6, and saturated NaHCO3 was added to pH 7. The reaction mixture was evaporated under reduced pressure and the residue coevaporated with toluene. The residue was then dissolved in EtOAc (150 mL) and washed 3× with saturated NaHCO3. The organic phase was evaporated and the residue purified by silica gel column chromatography using EtOAc-MeOH (95:5) as the eluent, yielding 3.85 g (78.3%) of product.

後処理

  1. additionwas added to pH 7
  2. customThe reaction mixture was evaporated under reduced pressure
  3. dissolutionThe residue was then dissolved in EtOAc (150 mL)
  4. washwashed 3× with saturated NaHCO3
  5. customThe organic phase was evaporated
  6. customthe residue purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-dccaeea032364ef2b81bc4d21d24b365
出典データセット
uspto-grants-1999_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05898031

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