HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-[(2,5-Dioxopyrrolidinyl)oxycarbonyloxy]ethyl cyclohexanecarboxylate → HCID 178473495, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-[(2,5-Dioxopyrrolidinyl)oxycarbonyloxy]ethyl cyclohexanecarboxylate | HCID 86610278 | — |
| Reactant | HCID 178511262 | HCID 178511262 | — |
| Solvent | MTBE acetone water | HCID 86610273 | — |
| Product | HCID 178473495 | HCID 178473495 | 26% |
Reaction Steps
Following the general nucleophilic carbamoylation procedure, tranexamic acid (780 mg, 5.0 mmol) and 1-[(2,5-dioxopyrrolidinyl)oxycarbonyloxy]ethyl cyclohexanecarboxylate (700 mg, 2.2 mmol) were reacted in the MTBE/acetone/water mixture (16 mL) to yield the title compound 22 (200 mg, 26% yield) as a white powder after work-up and mass-guided preparative HPLC purification. 1H NMR (400 MHz, DMSO-d6): δ=0.87-0.99 (m, 2H), 1.20-1.44 (br. m, 11H), 1.58-1.81 (m, 7H), 1.89-1.92 (m, 2H), 2.13 (tt, J=12, 3.6 Hz, 1H), 2.27-2.35 (m, 1H), 2.79-2.90 (m, 2H), 6.66 (q, J=5.6 Hz, 1H), 7.48 (t, J=6.0 Hz, 1H), 12.05 s, 1H). MS (ESI) m/z 378.13 (M+Na)+; 354.15 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08372881B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-028da0b5b8474b21b26f49bdff09a492 |
| Source note | uspto-grants-2013_02 |