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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501336Generated: November 4, 2026

Pyridine → HCID 86716509, compound

https://huagongshe.com/reaction/1501336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 86716510HCID 86716510—
SolventDichloromethaneHCID 6344—
ProductHCID 86716509HCID 86716509100%

Reaction Steps

To a solution of tert-butyl {1-[4-(6-amino-3-phenylimidazo[1,2-b]pyridazin-2-yl)phenyl]cyclobutyl}carbamate that was prepared in a manner analgous to that described for Intermediate Example Int-6.3 (0.10 g, 0.22 mmol) in DCM (4 mL) was added pyridine (0.036 mL, 0.44 mmol, 2 equiv) and acetic anhydride (0.027 mL, 0.29 mmol, 1.3 equiv). The reaction mixture was stirred for 24 h at room temperature, additional acetic anhydride (0.042 mL, 0.44 mmol, 2.0 equiv) was added and the reaction mixture was stirred at room temperature for an additional 24 h. The resulting mixture was concentrated under reduced pressure to give tert-butyl {1-[4-(6-acetamido-3-phenylimidazo[1,2-b]pyridazin-2-yl)phenyl]cyclobutyl}carbamate (0.11 g, 100%) which was used without further purification:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206185B2
Source datasetuspto-grants-2015_12
ORD IDord-3373d2e565fa4087b605e56ba75b38a4
Source noteuspto-grants-2015_12