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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339688Generated: October 29, 2026

Iodo benzene diacetate → HCID 67234327, compound

https://huagongshe.com/reaction/339688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodo benzene diacetateHCID 12217721—
ReactantN-[(E)-(8-bromo-6-fluoroquinolin-2-yl)methylideneamino]pyridin-2-amineHCID 68558317—
SolventDichloromethaneHCID 6344—
ProductHCID 67234327HCID 6723432774.4%

Reaction Conditions

Temperature23 °C

Reaction Steps

(E)-1-((8-Bromo-6-fluoroquinolin-2-yl)methylene)-2-(pyridin-2-yl)hydrazine (100 mg, 0.290 mmol) was weighed into a 25 mL 1 neck round bottom flask and suspended in 6.0 mL of DCM, followed by addition of iodobenzene diacetate (103 mg, 0.32 mmol). The reaction was stirred at 23° C. overnight, after which all starting materials had been consumed. The reaction was transferred to a separatory funnel and partitioned between 30 mL DCM and 30 mL Na2SO3, and the aqueous layer was washed with DCM. The combined organics were dried over magnesium sulfate and concentrated in vacuo to afford a white/yellow powder. The powder was triturated with 10 mL of anhydrous Et2O, affording the desired product as a white solid (74 mg, 74.4% yield). MS APCI (+) m/z 343 (M+1) detected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895550B2
Source datasetuspto-grants-2014_11
ORD IDord-7101884dfe4f4f8199659556a762a080
Source noteuspto-grants-2014_11