4,4-Diethoxybutylamine → HCID 90209396, compound
Reaction equation
[C:1]1([C@H:7]([NH:25][C:26]([O:28][C@@H:29]2[CH:34]3[CH2:35][CH2:36][N:31]([CH2:32][CH2:33]3)[CH2:30]2)=[O:27])[C:8]2[CH:9]=[C:10]([CH:22]=[CH:23][CH:24]=2)[O:11][CH2:12][C:13]2[CH:21]=[CH:20][C:16]([C:17](O)=[O:18])=[CH:15][CH:14]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[O:37]1[CH2:41][CH2:40][O:39][CH:38]1[C:42]1[CH:47]=[CH:46][C:45]([CH2:48][NH2:49])=[CH:44][CH:43]=1.C(OC(OCC)CCCN)C>>[N:31]12[CH2:32][CH2:33][CH:34]([CH2:35][CH2:36]1)[C@@H:29]([O:28][C:26](=[O:27])[NH:25][C@H:7]([C:8]1[CH:24]=[CH:23][CH:22]=[C:10]([O:11][CH2:12][C:13]3[CH:21]=[CH:20][C:16]([C:17](=[O:18])[NH:49][CH2:48][C:45]4[CH:44]=[CH:43][C:42]([CH:38]5[O:39][CH2:40][CH2:41][O:37]5)=[CH:47][CH:46]=4)=[CH:15][CH:14]=3)[CH:9]=1)[C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1)[CH2:30]2Participants
4
Procedure
The title was prepared as described in Example 5 Step 1 with 4-((3-((S)-phenyl((((R)-quinuclidin-3-yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoic acid and (4-(1,3-dioxolan-2-yl)phenyl)methanamine replacing 1-methyl-5-((3-((S)-phenyl((((R)-quinuclidin-3-yloxy)carbonyl)amino)methyl)phenoxy)methyl)-1H-pyrazole-3-carboxylic acid and 4-aminobutyraldehyde diethyl acetal respectively.
Workup
- customThe title was prepared
Sources & evidence
- ORD record
- ord-9a3fd4dd6b8240dc81d8e9de93f5695c
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08987299B2
Reaction notes
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