Ethyl 2-((tert-butoxycarbonyl)amino)acetate → HCID 68428757, compound
Reaction equation
[CH2:1]([O:3][C:4]([C:6]1[C:10]([C:11]([CH3:14])([CH3:13])[CH3:12])=[C:9]([Br:15])[N:8]([C:16]2[CH:21]=[CH:20][C:19]([F:22])=[CH:18][CH:17]=2)[C:7]=1[CH2:23]Br)=[O:5])[CH3:2].[CH2:25]([O:27][C:28](=[O:38])[CH2:29][NH:30][C:31]([O:33][C:34]([CH3:37])([CH3:36])[CH3:35])=[O:32])[CH3:26]>>[CH2:1]([O:3][C:4]([C:6]1[C:10]([C:11]([CH3:14])([CH3:13])[CH3:12])=[C:9]([Br:15])[N:8]([C:16]2[CH:21]=[CH:20][C:19]([F:22])=[CH:18][CH:17]=2)[C:7]=1[CH2:23][N:30]([C:31]([O:33][C:34]([CH3:35])([CH3:37])[CH3:36])=[O:32])[CH2:29][C:28]([O:27][CH2:25][CH3:26])=[O:38])=[O:5])[CH3:2]Participants
3
Procedure
Prepared in analogy to that of Example 1(c) from 5-bromo-2-bromomethyl-4-tert-butyl-1-(4-fluoro-phenyl)-1H-pyrrole-3-carboxylic acid ethyl ester and tert-butoxycarbonylamino-acetic acid ethyl ester. The title compound, ESI MS (m/z): 605 (M+Na+).
Sources & evidence
- ORD record
- ord-82c844de2fc5414b97ccaedbe6efef7b
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07696223B2
Reaction notes
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