反応式
[NH2:1][C:2]1[CH:15]=[CH:14][CH:13]=[CH:12][C:3]=1[C:4]([N:6]1[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1)=[O:5].[NH:16]1[CH2:21][CH2:20]C[CH2:18][CH2:17]1.C12C(=CC=CC=1)[NH:27]C(=O)OC2=O>>[NH:16]1[CH2:17][CH2:18][N:27]=[C:21]1[CH2:20][NH:1][C:2]1[CH:15]=[CH:14][CH:13]=[CH:12][C:3]=1[C:4]([N:6]1[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1)=[O:5]参加物
4
実験手順
1-(2-Aminobenzoyl)piperidine (prepared from piperidine and isatoic anhydride, using the methods described in Example 17) and CMI were reacted using conditions described in the general procedure for CMI coupling to give {2-[(4,5-dihydro-1H-imidazol-2-ylmethyl)amino]phenyl}(1-piperidinyl)methanone.
後処理
- customwere reacted
出典と根拠
- ORDレコード
- ord-c04a3bcf112440099fa5ff8ab35fe904
- 出典データセット
- uspto-grants-2005_04
- 特許番号
- US06884801B1
関連ノート
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