Hydrogen chloride-ethyl acetate → HCID 178479016, compound
Reaction equation
[NH:1]1[C:5]([C:6]2[CH:11]=[CH:10][C:9]([C:12]3([NH:15]C(=O)OC(C)(C)C)[CH2:14][CH2:13]3)=[CH:8][CH:7]=2)=[N:4][N:3]=[N:2]1.[ClH:23].C(OCC)(=O)C>C(OC(=O)C)C>[ClH:23].[NH:4]1[C:5]([C:6]2[CH:7]=[CH:8][C:9]([C:12]3([NH2:15])[CH2:13][CH2:14]3)=[CH:10][CH:11]=2)=[N:1][N:2]=[N:3]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To the solution of tert-butyl (1-(4-(1H-tetrazol-5-yl)phenyl)cyclopropyl)carbamate (D16) (800 mg, 2.65 mmol) in ethylacetate (10 ml), 4N HCl/ethyl acetate solution (20 ml) was added and the mixture was stirred at room temperature for 1 hour, then cooled to 0° C. The solid was filtered and washed with ethylacetate to afford the title compound (D17) (510 mg) as a yellow solid.
Workup
- temperaturecooled to 0° C
- filtrationThe solid was filtered
- washwashed with ethylacetate
Sources & evidence
- ORD record
- ord-61eb421ae0e840aeaca65dae7176814c
- Source dataset
- uspto-grants-2014_09
- Patent number
- US08828987B2
Reaction notes
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