HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 11439535, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N,N-Diethylethylenediamine | HCID 60993 | — |
| Reactant | HCID 86055263 | HCID 86055263 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 11439535 | HCID 11439535 | 73.7% |
Reaction Steps
7-fluoro-2,1,3-benzoselenadiazole-4-sulfonyl chloride (75 mg) was dissolved in 3 ml of acetonitrile. After the addition of N,N-diethylethylenediamine (22 mg) and triethylamine (351), the mixture was stirred on ice for 30 min. The reaction mixture was evaporated to dryness in vacuo and the residue was dissolved in CH2Cl2 and chromatographed on silica gel using CH2Cl2-CH3OH (93:7) to yield 7-fluoro-N-[2-(dimethylamino)ethyl]-2,1,3-benzoselenadiazole-4-sulfonamide (49 mg, 56%) as red powder. mp: 117-120° C. 1H-NMR δH8.09 (1H, d, J=7.5 Hz), 7.24 (1H, d, J=7.5 Hz), 2.93 (2H, t, J=6.7 Hz), 2.27 (2H, t, J=6.7 Hz), 1.98 (6H, s) in CD3OD; ESI-MSm/z 353 [(M+H)+]
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08796037B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-0c926c8d6ef64ecdbf28f79a6b1d6755 |
| Source note | uspto-grants-2014_08 |