HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-({[(2,5-Dioxopyrrolidin-1-yl)oxy]carbonyl}oxy)butyl butanoate → HCID 178454702, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-({[(2,5-Dioxopyrrolidin-1-yl)oxy]carbonyl}oxy)butyl butanoate | HCID 71427021 | — |
| Reactant | HCID 178511262 | HCID 178511262 | — |
| Solvent | MTBE acetone water | HCID 86610273 | — |
| Product | HCID 178454702 | HCID 178454702 | 27% |
Reaction Steps
Following the general nucleophilic carbamoylation procedure, tranexamic acid (800 mg, 5 mmol) and 1-[(2,5-dioxopyrrolidinyl)oxycarbonyloxy]butyl butanoate (700 mg, 2.3 mmol) were reacted in the MTBE/acetone/water mixture (16 mL) to yield the title compound 35 (210 mg, 27% yield) as a white powder after work-up and mass-guided preparative HPLC purification. 1H NMR (400 MHz, DMSO-d6): δ=0.87-0.95 (m, 8H), 1.22-1.41 (br. m, 5H), 1.56 (m, 2H), 1.68-1.73 (m, 4H), 1.89-1.92 (m, 2H), 2.13 (tt, J=12, 3.2 Hz, 1H), 2.30 (t, J=7.2 Hz, 2H), 6.65 (t, J=5.6 Hz, 1H), 7.45 (t, J=6.0 Hz, 1H), 12.04 (s, 1H). MS (ESI) m/z 366.21 (M+Na)+; 342.16 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07351740B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-9301fc42ac1f42ed946c4246a5217e22 |
| Source note | uspto-grants-2008_04 |