HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347525Generated: November 1, 2026
Azobisisobutyronitrile → HCID 21081533, compound
https://huagongshe.com/reaction/347525
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-Methyl-4-(methylsulfanyl)pyrrolo[2,1-f][1,2,4]triazine | HCID 21031512 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 21081533 | HCID 21081533 | 74% |
Reaction Steps
A solution of 5-methyl-4-methylsulfanyl-pyrrolo[2,1-f][1,2,4]triazine (200 mg, 1.12 mmol), NBS (218 mg, 1.23 mmol), and AIBN (spatula tip) in carbon tetrachloride (4 mL) was heated at 80° C. for 1 h. After cooling to rt, the solution was filtered to remove succinimide. To the filtrate was added 4-hydroxypiperidine (126 mg, 1.34 mmol, Aldrich) and DIPEA (214 μL, 1.23 mmol). The reaction was stirred at rt overnight and was then concentrated in vacuo. The residue was suspended in methanol and filtered. The filtrate was concentrated and the crude product was purified by flash chromatography on silica gel (20% MeOH/EtOAc) to give the title compound (229 mg, 74%) as a colorless solid. 1H NMR (DMSO-d6) δ 8.25 (s, 1H), 7.88 (d, 1H, J=2 Hz), 6.81 (d, 1H, J=2 Hz), 4.54 (br s, 1H), 3.76 (s, 2H), 3.48–3.44 (m, 1H), 2.75–2.71 (m, 2H), 2.62 (s, 3H), 2.10–2.08 (m, 2H), 1.70–1.68 (m, 2H), 1.38–1.36 (m, 2H); MS(ESI+) m/z 279.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07173031B2 |
|---|
| Source dataset | uspto-grants-2007_02 |
|---|
| ORD ID | ord-5baf4e2c0ada46eda99830f68dc2c639 |
|---|
| Source note | uspto-grants-2007_02 |
|---|