反応式
[C:1]1(C2SCC(C(O)=O)N=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.N1C2C(=CC(C#N)=CC=2)C=C1.[NH:26]1[C:34]2[C:29](=[CH:30][C:31]([C:35]3[S:36][CH2:37][C@@H:38]([C:40]([OH:42])=[O:41])[N:39]=3)=[CH:32][CH:33]=2)[CH:28]=[CH:27]1.[OH-].[Na+].[S:45](Cl)(Cl)(=[O:47])=[O:46].Cl>S([O-])(O)(=O)=O.C([N+](CCCC)(CCCC)CCCC)CCC.C1(C)C=CC=CC=1>[NH:26]1[C:34]2[C:29](=[CH:30][C:31]([C:35]3[S:36][CH2:37][C@@H:38]([C:40]([OH:42])=[O:41])[N:39]=3)=[CH:32][CH:33]=2)[CH:28]=[CH:27]1.[C:1]1([S:45]([N:26]2[C:34]3[C:29](=[CH:30][C:31]([C:35]4[S:36][CH2:37][C@@H:38]([C:40]([OH:42])=[O:41])[N:39]=4)=[CH:32][CH:33]=3)[CH:28]=[CH:27]2)(=[O:47])=[O:46])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1参加物
10
反応物 6
生成物 2
試薬・触媒・溶媒 2
実験手順
(R)-2-(1H-indol-5-yl)-4,5-dihydrothiazole-4-carboxylic acid 63a was synthesized using the same method as used for 42a from 1H-indole-5-carbonitrile and used without further purification. To a vigorously stirring solution of 63a (1 mmol) and tetrabutylammonium hydrogen sulfate (0.15 mmol) in toluene (10 mL) at 0° C. was added 50% aqueous sodium hydroxide (10 mL) and sulfonyl chloride (2 mmol). The resultant solution was stirred at RT for 6 h. Then 1 N HCl was added to acidify the mixture to pH=2 and extracted with CH2Cl2, the organic layer was separated and dried (MgSO4); then evaporated to dryness to yield 64a, which were used in subsequent steps without further purification.
後処理
- customused without further purification
- extractionextracted with CH2Cl2
- customthe organic layer was separated
- dry with materialdried (MgSO4)
- customthen evaporated to dryness
出典と根拠
- ORDレコード
- ord-9f1a7920997342cfa2aba54ae6ff5762
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08822513B2
関連ノート
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