HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 86048447, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Aziridine | HCID 9033 | — |
| Reactant | HCID 86048448 | HCID 86048448 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86048447 | HCID 86048447 | 84.3% |
Reaction Steps
A solution of 2-chloro-N-(6-hydroxyhexyl)-3,5-dinitrobenzamide (16) [for preparation see Example 14 below] (118 mg, 0.34 mmol) and Et3N (200 mg) in EtOAc (200 mL) was treated with aziridine (100 mg) at room temperature for 3 h. The mixture was diluted with EtOAc and washed three times with water, after dry, concentrated under reduced pressure until about 20 mL, the yellow solid was collected and gave 101 mg product (84%); 1H NMR [(CD3)2SO] δ 8.74 (d, J=2.8 Hz, 1 H), 8.63 (m, 1 H), 8.29 (d, J=2.8 Hz, 1 H), 4.31 (m, 1 H), 3.39 (m, 2 H), 3.25 (m, 2 H), 2.37 (s, 4 H), 1.56 (m, 2 H), 1.43 (m, 2 H), 1.33 (m, 4 H). Anal. (C15H20N4O6) C, H, N.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07629332B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-79ff7128d62847659b01a55b63d70328 |
| Source note | uspto-grants-2009_12 |