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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272335Generated: November 1, 2026

5-Bromo-2-fluoropyridine → 3-(6-Fluoropyridine-3-yl)-5-(4-(4-methoxyphenyl)piperazin-1-yl)-2,2,4,6,7-pentamethyl-2,3-dihydro-1-benzofuran-3-ol

https://huagongshe.com/reaction/1272335

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-fluoropyridineHCID 2783168—
Reactant5-[4-(4-methoxyphenyl)piperazin-1-yl]-2,2,4,6,7-pentamethyl-1-benzofuran-3(2H)-oneHCID 22935595—
Product3-(6-Fluoropyridine-3-yl)-5-(4-(4-methoxyphenyl)piperazin-1-yl)-2,2,4,6,7-pentamethyl-2,3-dihydro-1-benzofuran-3-olHCID 5884733167%

Reaction Steps

Using 4-(4-methoxyphenyl)-1-(2,2,4,6,7-pentamethyl-2,3-dihydro-1-benzofuran-3-on-5-yl)piperazine and 5-bromo-2-fluoropyridine obtained in Reference Example 13, the title compound was obtained in the same manner as in Example 33. Yield 67% mp. 129–131° C. (hexane-ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208495B2
Source datasetuspto-grants-2007_04
ORD IDord-a15879dd9874455a8fe9c8121c092aa1
Source noteuspto-grants-2007_04