反応式
[CH:1]1([C:11]([OH:13])=O)[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][CH2:2]1.[NH2:14][C:15]1[CH:16]=[CH:17][C:18]([CH:21]([CH3:23])[CH3:22])=[N:19][CH:20]=1>>[CH:21]([C:18]1[N:19]=[CH:20][C:15]([NH:14][C:11]([CH:1]2[C:10]3[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=3)[CH2:4][CH2:3][CH2:2]2)=[O:13])=[CH:16][CH:17]=1)([CH3:23])[CH3:22]参加物
3
実験手順
By the reaction and treatment in the same manner as in Preparation Example 11 using 1,2,3,4-tetrahydronaphthalene-1-carboxylic acid (1.51 g) and 5-amino-2-isopropylpyridine (1.17 g) as starting materials, N-(6-isopropylpyridin-3-yl)-1,2,3,4-tetrahydronaphthalene-1-carboxamide (2.18 g) was obtained. melting point: 155.7° C.
後処理
- customBy the reaction and treatment in the same manner
出典と根拠
- ORDレコード
- ord-059f4241356a4b3eacb0ba0fe5a8db36
- 出典データセット
- uspto-grants-2012_06
- 特許番号
- US08198454B2
関連ノート
読み込み中…