Hydrochloric Acid → 1251925-09-3
Reaction equation
C([N:14]1[CH2:17][CH:16]([N:18]2[CH:22]=[N:21][CH:20]=[N:19]2)[CH2:15]1)(C1C=CC=CC=1)C1C=CC=CC=1.[ClH:23]>C(O)C.[Pd]>[ClH:23].[N:18]1([CH:16]2[CH2:17][NH:14][CH2:15]2)[CH:22]=[N:21][CH:20]=[N:19]1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a mixture of N-benzhydryl-3-(1,2,4-triazol-1-yl) azetidine (0.6 g) in 20 ml of ethanol was added 2 ml of 1N hydrochloric acid followed by the addition of 0.6 g of Pd/C (10%). The mixture was hydrogenated at 50 psi for two days. After filtration and evaporation, the crude product was crystallized from methanol-ether to afford 0.235 g of white solid. 1H NMR (D2O) δ: 9.14 (S, 1H), 8.57 (S, 1H), 5.97 (m, 1H), 4.8-4.5 (m, 4H).
Workup
- filtrationAfter filtration and evaporation
- customthe crude product was crystallized from methanol-ether
Sources & evidence
- ORD record
- ord-86930354c3be4432a7504a8f6701c0e9
- Source dataset
- uspto-grants-1994_08
- Patent number
- US05342846
Reaction notes
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