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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509548Generated: November 2, 2026

Azobisisobutyronitrile → HCID 68104457, compound

https://huagongshe.com/reaction/509548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 68088706HCID 68088706—
SolventEthyl AcetateHCID 8857—
ProductHCID 68104457HCID 68104457—

Reaction Conditions

Temperature85 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096584B2
Source datasetuspto-grants-2015_08
ORD IDord-0d4146b4d75c4a51ba9a6aea68af58fd
Source noteuspto-grants-2015_08