反応式
[CH3:1][NH:2][C@H:3]1[CH2:8][CH2:7][C@H:6]([CH2:9][CH2:10][CH2:11][CH2:12][CH2:13]OS(C)(=O)=O)[CH2:5][CH2:4]1.FC(F)(F)C(O)=O.Cl[C:27]([O:29][C:30]1[CH:35]=[CH:34][C:33]([Br:36])=[CH:32][CH:31]=1)=[O:28].[CH2:37]([NH:39][CH2:40][CH2:41][OH:42])[CH3:38]>>[Br:36][C:33]1[CH:34]=[CH:35][C:30]([O:29][C:27](=[O:28])[N:2]([C@H:3]2[CH2:4][CH2:5][C@H:6]([CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][N:39]([CH2:37][CH3:38])[CH2:40][CH2:41][OH:42])[CH2:7][CH2:8]2)[CH3:1])=[CH:31][CH:32]=1参加物
5
実験手順
In analogy to examples 29.10 and 29.11, trans-Methansulfonic acid 5-(4-methyl amino-cyclohexyl)-pentyl ester.trifluoroacetic acid salt and 4-bromophenyl chloroformate were reacted, followed by treatment with by 2-ethylamino-ethanol to yield trans-(4-{5-[Ethyl-(2-hydroxy-ethyl)-amino]-pentyl}-cyclohexyl)-methyl-carbamic acid 4-bromo-phenyl ester, MS: 469 (MH+, 1Br).
出典と根拠
- ORDレコード
- ord-9d8dcf7ce4c24d7a9a406f0ba96f686c
- 出典データセット
- uspto-grants-2005_02
- 特許番号
- US06858651B2
関連ノート
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