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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676257Generated: November 1, 2026

3-Fluoro-4-((2-iodothieno[3,2-b]pyridin-7-yl)oxy)aniline → HCID 67348983, compound

https://huagongshe.com/reaction/1676257

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluoro-4-((2-iodothieno[3,2-b]pyridin-7-yl)oxy)anilineHCID 58474950—
ReactantHCID 60768076HCID 60768076—
ProductHCID 67348983HCID 67348983—

Reaction Conditions

Temperature50 °C

Reaction Steps

Prepared from N,N-dimethyl-1-(prop-2-ynyl)piperidin-4-amine (32 mg, 0.19 mmol) and 3-fluoro-4-(2-iodothieno[3,2-b]pyridin-7-yloxy)benzenamine (Example 6, Step A; 50 mg, 0.13 mmol) according to the procedure described for Example 6, Step B, except the reaction was heated at 50° C. for 7 hours. The crude was partially purified by preparative TLC [5% MeOH (containing 7N NH3) in CH2Cl2]. The product was obtained as a waxy solid (34 mg, 31%; 50% purity by 1H NMR), and carried forward without further purification. LRMS (APCI pos) m/e 425 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003662B2
Source datasetuspto-grants-2011_08
ORD IDord-e39edb0c2b8546fba0c8c0d07c858e75
Source noteuspto-grants-2011_08