(4S)-6-Azaspiro[2.5]octan-4-ol → Hydrochloric Acid
Reaction equation
[CH3:1][O:2][C:3](=[O:23])[C@@H:4]([N:8]1[C:14](=[O:15])[CH2:13][CH2:12][N:11]([C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([Cl:22])[CH:17]=2)[CH2:10][CH2:9]1)[CH2:5][CH:6]=O.[CH2:24]1[C:26]2([CH2:31][CH2:30][NH:29][CH2:28][C@H:27]2[OH:32])[CH2:25]1>>[ClH:22].[CH3:1][O:2][C:3](=[O:23])[C@@H:4]([N:8]1[C:14](=[O:15])[CH2:13][CH2:12][N:11]([C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([Cl:22])[CH:17]=2)[CH2:10][CH2:9]1)[CH2:5][CH2:6][N:29]1[CH2:30][CH2:31][C:26]2([CH2:24][CH2:25]2)[C@H:27]([OH:32])[CH2:28]1Participants
4
Reactant 2
Product 2
Procedure
In analogy to the procedure described in example 1K, (S)-2-[4-(3-chloro-phenyl)-7-oxo-[1,4]diazepan-1-yl]-4-oxo-butyric acid methyl ester and (S)-6-aza-spiro[2.5]octan-4-ol; hydrochloride (intermediate 2) gave the title compound as light yellow foam. MS: 450.3 (MH+, 1Cl).
Sources & evidence
- ORD record
- ord-f20a309fcfda4a1bb2ebd5035412f604
- Source dataset
- uspto-grants-2012_03
- Patent number
- US08138175B2
Reaction notes
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