HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509548Generated: November 2, 2026
Azobisisobutyronitrile → HCID 68104457, compound
https://huagongshe.com/reaction/509548
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 68088706 | HCID 68088706 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 68104457 | HCID 68104457 | — |
Reaction Steps
tert-Butyl N-tert-butoxycarbonyl-N-[5-(5-isopropylsulfonyl-2-pyridyl)-3-[3-(p-tolyl)isoxazol-5-yl]-2-pyridyl]carbamate (245 mg, 0.3860 mmol) was suspended in EtOAc (2.5 mL) followed by the addition of NBS (89.31 mg, 0.5018 mmol) and AIBN (6.338 mg, 0.03860 mmol). The mixture was heated to 85° C. and placed under a bright lamp for 2 hours. The reaction mixture was cooled to ambient temperature and washed with saturated aqueous NaHCO3/brine (1:1, ×2), dried (MgSO4), filtered and concentrated in vacuo to give the impure sub-title compound as a pale brown foam. This was used in the next step without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09096584B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-0d4146b4d75c4a51ba9a6aea68af58fd |
|---|
| Source note | uspto-grants-2015_08 |
|---|