HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 11078903, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyl succinimido carbonate | HCID 83172 | — |
| Reactant | HCID 11010525 | HCID 11010525 | — |
| Reactant | HCID 11101150 | HCID 11101150 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11078903 | HCID 11078903 | — |
Reaction Steps
1-Benzyloxycarbonyl-4-(ethoxycarbonyl)-4-(2-oxopiperidino)-piperidine. 4-(Ethoxycarbonyl)-4-(2-oxopiperidino)piperidine (9.0 g) in dichloromethane (25 mL) was added to a solution of N-(benzyloxycarbonyloxy)succinimide (8.8 g) and triethylamine (5.4 mL) in dichloromethane (150 mL). After 1.5 hours, the reaction mixture was washed successively with 1.0N hydrochloric acid and saturated aqueous sodium bicarbonate. The separated organic layer was dried and evaporated to give the title compound (11.6 g) as a light yellow solid; MS: m/z=389(M+1); NMR (CDCl3 /CF3COOH): 7.37 (m,5), 5.16 (s,2), 4.28 (q,2, J=7.1), 4.09 (m,2), 3.40 (m,2), 3.28 (m,2), 2.53 (m,2), 2.34 (m,2), 1.83 (m,6), 1.30 (t,3, J=7.1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05677317 |
| Source dataset | uspto-grants-1997_10 |
| ORD ID | ord-9cb28b698dcc42a29091d6c7847cccb4 |
| Source note | uspto-grants-1997_10 |