HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 7-Bromo-1,2,3-benzothiadiazol-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | benzo[d][1,2,3]thiadiazol-4-aMine | HCID 21936630 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-Bromo-1,2,3-benzothiadiazol-4-amine | HCID 66760437 | 30% |
Reaction Steps
A mixture of 1,2,3-benzothiadiazol-4-amine (200.0 mg, 1.323 mmol) and NBS (341.4 mg, 1.918 mmol) in THF (10 mL) was stirred at RT overnight. The solution was adsorbed onto silica gel and purified by ISCO chromatography (10 to 30% EtOAc:heptane) to afford 80 mg (30%) of the title compound as a yellow solid. 1H NMR (400 MHz, DMSO-d6): δ 6.74 (d, J=8.3 Hz, 1 H), 6.97 (s, 2 H), 7.60 (d, J=8.3 Hz, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08378104B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-4b16701705834caabacd0ca970e00cf2 |
| Source note | uspto-grants-2013_02 |