Hydrochloric Acid → HCID 178478702, compound
Reaction equation
C1(C(C2C=CC=CC=2)(C2C=CC=CC=2)[N:8]2[CH:12]=[C:11]([C@@H:13]3[CH2:15][C@H:14]3[CH2:16][NH2:17])[N:10]=[CH:9]2)C=CC=CC=1.[ClH:30]>CO>[ClH:30].[ClH:30].[NH2:17][CH2:16][C@@H:14]1[CH2:15][C@H:13]1[C:11]1[N:10]=[CH:9][NH:8][CH:12]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
To a solution of N-triphenylmethyl-4-(trans-2-aminomethyl-cyclopropyl)imidazole (100 mg, 0.26 mmol) in methanol (15 mL) was added 2N HCl solution (2.5 mL). The mixture was stirred at 60° C. for 2 hours and then concentrated. The resulting residue was extracted with ether (3×20 ml). The aqueous layer was lyophilized to give the product (47 mg, 83% yield).
Workup
- concentrationconcentrated
- extractionThe resulting residue was extracted with ether (3×20 ml)
Sources & evidence
- ORD record
- ord-b4fac3a3f7af44e7b443dac7fa09548e
- Source dataset
- uspto-grants-2004_09
- Patent number
- US06794405B2
Reaction notes
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