Hydrochloric Acid → 3-(5H-tetrazol-5-yl)morpholine hydrochloride
Reaction equation
[N:1]1[CH:5]([CH:6]2[CH2:11][O:10][CH2:9][CH2:8][N:7]2C(OC(C)(C)C)=O)[N:4]=[N:3][N:2]=1.[ClH:19]>CCOC(C)=O>[ClH:19].[N:4]1[CH:5]([CH:6]2[CH2:11][O:10][CH2:9][CH2:8][NH:7]2)[N:1]=[N:2][N:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Tert-butyl 3-(5H-tetrazol-5-yl)morpholine-4-carboxylate (2 g, 7.8 mmol) was reacted with a solution of HCl in EtOAc (6 mol/L, 30 mL) according to the procedure as described in Example 18, Step B to give the title compound as a grey solid (1.05 g, 70%). The compound was characterized by the following spectroscopic data:
Sources & evidence
- ORD record
- ord-6e912af3ea4548d89de5bb12d015fa50
- Source dataset
- uspto-grants-2016_05
- Patent number
- US09340538B2
Reaction notes
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