HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 86744569, compound → HCID 67830825, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 86744569 | HCID 86744569 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 67830825 | HCID 67830825 | — |
Reaction Steps
A solution of cis-N-(Benzyloxycarbonyl) azetidine 2,3-dicarboxylic acid and, e.g., ammonia are reacted with [(CH3)2N]3PCl2 to form the cis-N(benzyloxycarbonyl)azetidine-2,3-dicarboxamide (XI), as set forth by Appel et al., Chem. Ber. 116, 2037-2040 (1983). XI, 10% Pd/C and methanol are hydrogenated in a Parr shaker under 3 atm of hydrogen, for 4 hours. The catalyst is filtered off and thoroughly washed. The solution is evaporated to dryness and dried in vacuo to arrive at cis-azetidine-2,3-dicarboxamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04946839 |
| Source dataset | uspto-grants-1990_08 |
| ORD ID | ord-ad6f3563222c49a0948480dc4816d912 |
| Source note | uspto-grants-1990_08 |