1-Boc-4-(3-[(2-chloro-pyridine-3-carbonyl)-amino]-5-trifluoromethyl-phenoxy}-piperidine → N-[4-tert-Butyl-3-(1-methyl-piperidin-4-ylmethoxy)-phenyl]-2-chloro-nicotinamide
反応式
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([NH2:11])=[CH:7][C:6]=1[O:12][CH2:13][CH:14]1[CH2:19][CH2:18][N:17]([CH3:20])[CH2:16][CH2:15]1)([CH3:4])([CH3:3])[CH3:2].C(N1CCC(OC2C=C(C(F)(F)F)C=C(N[C:46]([C:48]3[C:49]([Cl:54])=[N:50][CH:51]=[CH:52][CH:53]=3)=[O:47])C=2)CC1)(OC(C)(C)C)=O>>[C:1]([C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:46](=[O:47])[C:48]2[CH:53]=[CH:52][CH:51]=[N:50][C:49]=2[Cl:54])=[CH:7][C:6]=1[O:12][CH2:13][CH:14]1[CH2:19][CH2:18][N:17]([CH3:20])[CH2:16][CH2:15]1)([CH3:4])([CH3:2])[CH3:3]参加物
3
実験手順
N-[4-tert-Butyl-3-(1-methyl-piperidin-4-ylmethoxy)-phenyl]-2-chloro-nicotinamide was prepared from 4-tert-butyl-3-(1-methyl-piperidin-4-ylmethoxy)-phenylamine by a procedure similar to that described in the preparation of 1-Boc-4-{3-[(2-chloro-pyridine-3-carbonyl)-amino]-5-trifluoromethyl-phenoxy}-piperidine.
出典と根拠
- ORDレコード
- ord-7fc1c4e6ac5a465789f60aa07a77a467