1-Tetrazolylacetic acid → HCID 66976208, compound
Reaction equation
[NH2:1][CH2:2][C@H:3]1[C@H:9]([C:10]2[CH:15]=[CH:14][C:13]([Cl:16])=[C:12]([Cl:17])[CH:11]=2)[O:8][CH2:7][CH2:6][N:5](C(OC(C)(C)C)=O)[CH2:4]1.[N:25]1([CH2:30][C:31](O)=[O:32])[CH:29]=[N:28][N:27]=[N:26]1>>[ClH:16].[Cl:17][C:12]1[CH:11]=[C:10]([C@@H:9]2[O:8][CH2:7][CH2:6][NH:5][CH2:4][C@H:3]2[CH2:2][NH:1][C:31](=[O:32])[CH2:30][N:25]2[CH:29]=[N:28][N:27]=[N:26]2)[CH:15]=[CH:14][C:13]=1[Cl:16]Participants
3
Procedure
Using tert-butyl (6R,7R)-6-(aminomethyl)-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylate and 2-(1H-tetrazol-1-yl)acetic acid, and by a method similar to that in Example 39, steps A and B, the title compound was obtained.
Sources & evidence
- ORD record
- ord-36de037bb4f647b6b4364dd8a01cd2e7
- Source dataset
- uspto-grants-2014_05
- Patent number
- US08722662B2
Reaction notes
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