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

Sodium Bicarbonate → [2-(5-{1-[3-chloro-4-(methylsulfonyl)phenyl]-2-[(2R,3R,7R)-2,3-diphenyl-1,4-dioxaspiro[4.4]non-7-yl]ethyl}-1H-pyrrol-2-yl)-1,3-thiazol-5-yl]methanol

HRID 1882078
ノート
印刷プレビュー

反応式

HRID 1882078 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH:12]([CH2:32][C@H:33]2[CH2:53][CH2:52][C:35]3([O:39][C@H:38]([C:40]4[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=4)[C@@H:37]([C:46]4[CH:51]=[CH:50][CH:49]=[CH:48][CH:47]=4)[O:36]3)[CH2:34]2)[C:13](=O)[CH2:14][CH2:15][C:16]([C:18]2[S:19][C:20]([CH2:23][O:24]C3CCCCO3)=[CH:21][N:22]=2)=O)[CH:5]=[CH:6][C:7]=1[S:8]([CH3:11])(=[O:10])=[O:9].C([O-])(=O)C.[NH4+:58].C(=O)([O-])O.[Na+]>C(O)(=O)C.C(OCC)(=O)C>[Cl:1][C:2]1[CH:3]=[C:4]([CH:12]([C:13]2[NH:58][C:16]([C:18]3[S:19][C:20]([CH2:23][OH:24])=[CH:21][N:22]=3)=[CH:15][CH:14]=2)[CH2:32][C@H:33]2[CH2:53][CH2:52][C:35]3([O:36][C@H:37]([C:46]4[CH:47]=[CH:48][CH:49]=[CH:50][CH:51]=4)[C@@H:38]([C:40]4[CH:41]=[CH:42][CH:43]=[CH:44][CH:45]=4)[O:39]3)[CH2:34]2)[CH:5]=[CH:6][C:7]=1[S:8]([CH3:11])(=[O:10])=[O:9]
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

6

反応物 3

HCID 516892Sodium BicarbonateHCID 517165Ammonium AcetateHCID 59331390HCID 59331390、化合物

生成物 1

HCID 59331362[2-(5-{1-[3-chloro-4-(methylsulfonyl)phenyl]-2-[(2R,3R,7R)-2,3-diphenyl-1,4-dioxaspiro[4.4]non-7-yl]ethyl}-1H-pyrrol-2-yl)-1,3-thiazol-5-yl]methanol収率 42%

試薬・触媒・溶媒 2

HCID 176
Acetic Acid
溶媒
HCID 8857Ethyl Acetate溶媒

反応条件

温度
110 °C

実験手順

To a solution of 5-[3-chloro-4-(methylsulfonyl)phenyl]-6-[(2R,3R,7R)-2,3-diphenyl-1,4-dioxaspiro[4.4]non-7-yl]-1-{5-[(tetrahydro-2H-pyran-2-yloxy)methyl]-1,3-thiazol-2-yl}hexane-1,4-dione (416 mg) in acetic acid (2.5 mL) was added ammonium acetate (659 mg), and the mixture was stirred at 110° C. for 1 hr. After cooling to room temperature, the mixture was neutralized with saturated aqueous sodium hydrogen carbonate solution. The reaction mixture was diluted with ethyl acetate and washed with water. The ethyl acetate layer was dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography, and the title compound (151 mg, yield 42%) was obtained as a pale-yellow amorphous solid from a fraction eluted with ethyl acetate-hexane (19:1, volume ratio). MS: 675 (MH+).

後処理

  1. temperatureAfter cooling to room temperature
  2. washwashed with water
  3. dry with materialThe ethyl acetate layer was dried (MgSO4)
  4. concentrationconcentrated

出典と根拠

ORDレコード
ord-aacf1eea28db42ca99e9ddb312930bbc
出典データセット
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08318746B2

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