HuagongsheHuagongshe Chemistry Print Report · For research reference only
benzyl 3-(1-methyl-1H-benzimidazol-2-yl)azetidine-1-carboxylate → 2-(azetidin-3-yl)-1-methyl-1H-1,3-benzodiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | benzyl 3-(1-methyl-1H-benzimidazol-2-yl)azetidine-1-carboxylate | HCID 89486757 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(azetidin-3-yl)-1-methyl-1H-1,3-benzodiazole | HCID 89488176 | — |
Reaction Steps
A solution of 1-3 (3.32 g, 10.33 mmol) in MeOH (52 mL) was subjected to 2 cycles of the evacuation/backfilling with nitrogen and then treated with 10% Pd/C (1.1 g). The evacuation/backfilling with nitrogen procedure was repeated two times and then the nitrogen atmosphere was exchanged for a hydrogen atmosphere by evacuation/backfilling with a balloon of hydrogen. After stirring for 3 h under hydrogen at room temperature, the reaction mixture was filtered through celite, and washed with additional MeOH (20 mL). The filtrate was concentrated to yield Intermediate 1 as brown solid. MS: m/z=188.2 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09428492B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-ce098ffee9f4440a9010fbd602c7643d |
| Source note | uspto-grants-2016_08 |