HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → 1,1-Dimethylethyl 4-[2-(3-azetidinyloxy)phenyl]-1-piperazinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 69420117 | HCID 69420117 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1,1-Dimethylethyl 4-[2-(3-azetidinyloxy)phenyl]-1-piperazinecarboxylate | HCID 69417314 | 76% |
Reaction Steps
4-[2-(1-Benzhydryl-azetidin-3-yloxy)-phenyl]-piperazine-1-carboxylic acid tert-butyl ester (750 mg, 1.5 mmol) and ammonium formate (1.8 g, 30 mmol) were dissolved into methanol (50 mL) at r.t. The solution was added slowly to 10% palladium on carbon (750 mg) in methanol (20 mL) under nitrogen atmosphere. The mixture was stirred for about 48 hours and filtered through a bed of celite. The solvent was removed under reduced pressure to afford the title compound as a colorless oil (380 mg, 60%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07186715B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-b2922be5e8e14ed58c3cd708e84c3137 |
| Source note | uspto-grants-2007_03 |