反応式
N[C:2]1S[C:4]([CH2:12][CH3:13])=[CH:5][C:6]=1C(OCC)=O.[C:14]([C:19]1[CH:23]=[C:22]([CH2:24][CH3:25])[S:21][C:20]=1[NH:26][C:27](=[O:31])[CH:28]([CH3:30])[CH3:29])([O:16][CH2:17][CH3:18])=[O:15].C(I)CCCCC>>[CH2:13]([N:26]([C:20]1[S:21][C:22]([CH2:24][CH3:25])=[CH:23][C:19]=1[C:14]([O:16][CH2:17][CH3:18])=[O:15])[C:27](=[O:31])[CH:28]([CH3:29])[CH3:30])[CH2:12][CH2:4][CH2:5][CH2:6][CH3:2]参加物
4
実験手順
Ethyl 2-amino-5-ethyl-3-thiophenecarboxylate (Chemische Berichte 99, 94 (1966)) was converted into N-(3-carbethoxy-5-ethyl-2-thienyl)-2-methylpropanamide by the method described in Example 41. Alkylation of the unpurified product with n-hexyl iodide as described in Example 43 gave the title compound as a light yellow oil, b.p. 145°-147° C./0.25 mm. NMR showed that the material was the correct product.
出典と根拠
- ORDレコード
- ord-680c2569482649099319afa0ce136218
- 出典データセット
- uspto-grants-1980_09
- 特許番号
- US04222946
関連ノート
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