Hydrochloric Acid → 5-(3,5-Dimethyl-benzylcarbamoyl)-thiophene-3-carboxylic acid ethyl ester
反応式
[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[C:8]([C:11]([OH:13])=O)[S:9][CH:10]=1)=[O:5])[CH3:2].CN(C)CCCN=C=NCC.Cl.[CH3:26][C:27]1[CH:28]=[C:29]([CH:32]=[C:33]([CH3:35])[CH:34]=1)[CH2:30][NH2:31]>C(Cl)Cl>[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[C:8]([C:11](=[O:13])[NH:31][CH2:30][C:29]2[CH:32]=[C:33]([CH3:35])[CH:34]=[C:27]([CH3:26])[CH:28]=2)[S:9][CH:10]=1)=[O:5])[CH3:2]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
0.5 g 2-carboxy-thiophen-4-carboxylic acid ethyl ester (M. Janda, J. Srogl, M. Nemec, I. Stibor; Org. Prep. and Proced. Int. 3 (6) (1971) 295.) and 0.67 g N′-(3-dimethylaminopropyl)-N-ethylcarbodiimid×HCl are stirred in 50 mL DCM for 15 min. Then, 0.338 g 3,5-dimethylbenzylamin are added and the mixture is stirred overnight. The solution is extracted with 2N HCl and water, then evaporated. The residue is titurated with isohexan, and the resulting crystals are filtrated and air-dried, yielding 0.58 g (73%) crude 5-(3,5-Dimethyl-benzylcarbamoyl)-thiophene-3-carboxylic acid ethyl ester (7b). This ester in converted to title compound by reaction with hydroxylamine hydrochloride in a manner similar to that described for the conversion of 4b into 4a in example 4. After chromatography (silica, ethylacetate), thiophene-2,4-dicarboxylic acid 2-(3,5-dimethyl-benzylamide) 4-hydroxyamide (7a) is obtained as crystals; 44 mg, 9%, mp: 181° C. (decomp.).
後処理
- extractionThe solution is extracted with 2N HCl and water
- customevaporated
- filtrationthe resulting crystals are filtrated
- customair-dried
出典と根拠
- ORDレコード
- ord-84921da024c8432f9171f14d453d8926
- 出典データセット
- uspto-grants-2004_08
- 特許番号
- US06784173B2
反応ノート
読み込み中…