HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aziridine → HCID 11290689, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aziridine | HCID 9033 | — |
| Reactant | HCID 11404780 | HCID 11404780 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11290689 | HCID 11290689 | 84% |
Reaction Steps
A stirred solution of the above amide (315 mg, 0.95 mmol) in CH2Cl2 (35 mL) was treated with aziridine (197 μL, 3.81 mmol) at room temperature for 8 h. The mixture was partitioned between more CH2Cl2 and water, and the organic layer was dried and concentrated under reduced pressure. The residue was dissolved in EtOAc and filtered through a short column of silica gel to give 8 (269 mg, 84%): mp (CH2Cl2/iPr2O) 137° C.; 1H NMR [(CD3)2SO] δ8.86 (t, J=5.6 Hz, 1 H, NH), 8.66 (s, 1H, H-3), 7.40 (s, 1H, H-6), 3.63 (s, 3H, Me), 3.51-3.43 (m, 2H, NHCH2), 2.61 (t, J=6 8 Hz, 2H, CH2CO), 2 48 (s, 4H, aziridine-H). Anal. Calcd for C13H14N4O7: C, 46.15;H, 4 17; N, 16 57. Found: C, 45.89,H, 3.89; N, 16.45%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06517836B1 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-6a6ff077b85a4b75840ba69f52bb6406 |
| Source note | uspto-grants-2003_02 |