Hydrochloric Acid → HCID 90203590, compound
Reaction equation
[C:1]([C@H:4]1[N:8](C(OC(C)(C)C)=O)[C:7]([CH3:17])([CH3:16])[CH2:6][CH2:5]1)(=[O:3])[NH2:2].[ClH:18]>O1CCOCC1>[ClH:18].[CH3:16][C:7]1([CH3:17])[NH:8][C@H:4]([C:1]([NH2:2])=[O:3])[CH2:5][CH2:6]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In analogy to the procedure described in Example 82 a), (S)-tert-butyl 5-carbamoyl-2,2-dimethylpyrrolidine-1-carboxylate (CAN 1292838-05-1) was treated with a 4 M solution of HCl in dioxane to give the title compound as colorless solid which was sufficiently pure to be used in the next step; MS (EI): m/e=143.2 [(M-Cl)H+].
Sources & evidence
- ORD record
- ord-3dbf7fd3a93e471292f22a33c97388dc
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09303012B2
Reaction notes
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