Hydrochloric Acid → (S)-2-(2-(Methoxymethyl)pyrrolidin-1-yl)ethanamine
Reaction equation
[CH3:1][O:2][CH2:3][C@@H:4]1[CH2:8][CH2:7][CH2:6][N:5]1[CH2:9][CH2:10][NH:11]C(=O)OC(C)(C)C.Cl>CO>[CH3:1][O:2][CH2:3][C@@H:4]1[CH2:8][CH2:7][CH2:6][N:5]1[CH2:9][CH2:10][NH2:11]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of (S)-tert-butyl 2-(2-(methoxymethyl)pyrrolidin-1-yl)ethylcarbamate (step 1) (1.89 g, 7.32 mmol) and in MeOH (5 ml) and treated with 2M HCl in MeOH (10 equivalents) at room temperature over the weekend. The solvent was removed in vacuo to afford the title compound;
Workup
- customThe solvent was removed in vacuo
Sources & evidence
- ORD record
- ord-1c802c2680ba4f128f90f4fbd50fe2b7
- Source dataset
- uspto-grants-2014_11
- Patent number
- US08883819B2
Reaction notes
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