HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-({[(2,5-Dioxopyrrolidin-1-yl)oxy]carbonyl}oxy)butyl benzoate → HCID 178453627, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-({[(2,5-Dioxopyrrolidin-1-yl)oxy]carbonyl}oxy)butyl benzoate | HCID 71427020 | — |
| Reactant | HCID 178511262 | HCID 178511262 | — |
| Solvent | MTBE acetone water | HCID 86610273 | — |
| Product | HCID 178453627 | HCID 178453627 | 19% |
Reaction Steps
Following the general nucleophilic carbamoylation procedure, tranexamic acid (800 mg, 5 mmol) and 1-[(2,5-dioxopyrrolidinyl)oxycarbonyloxy]butyl benzoate (700 mg, 2.1 mmol) were reacted in the MTBE/acetone/water mixture (16 mL) to yield the title compound 39 (150 mg, 19% yield) as a white powder after work-up and mass-guided preparative HPLC purification. 1H NMR (400 MHz, DMSO-d6): δ=0.84-0.99 (m, 5H), 1.20-1.38 (br. m, 3H), 1.41-1.51 (m, 2H), 1.70-1.73 (m, 2H), 1.84-1.89 (m, 4H), 2.11 (tt, J 12, 3.2 Hz, 1H), 2.82-2.91 (m, 2H), 6.61 (t, J=5.6 Hz, 1H), 7.52-7.58 (m, 3H), 7.47 (t, J=6.0 Hz, 1H), 7.95-7.97 (m, 2H), 12.04 (s, 1H). MS (ESI) m/z 400.15 (M+Na)+; 376.16 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08372881B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-c021c029e5464f4c8262127e6d0dc647 |
| Source note | uspto-grants-2013_02 |