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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190677Generated: October 30, 2026

3-Fluorophenylboronic acid → HCID 59317980, compound

https://huagongshe.com/reaction/2190677

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluorophenylboronic acidHCID 2733986—
Reactant5'-(3-iodo-4-methyl-phenylcarbamoyl)-3,4,5,6-tetrahydro-2H-[1,2]bipyridinyl-4 carboxylic acid ethyl esterHCID 59318057—
Reactant5'-(2-methyl-biphenyl-4-ylcarbamoyl)-3,4,5,6-tetrahydro-2H-[1,2]bipyridinyl-4-carboxylic acid ethyl esterHCID 59318171—
ProductHCID 59317980HCID 59317980—

Reaction Steps

5′-(3′-Fluoro-6-methyl-biphenyl-3-ylcarbamoyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-4-carboxylic acid ethyl ester was prepared from 5′-(3-iodo-4-methyl-phenylcarbamoyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-4 carboxylic acid ethyl ester and 3-fluorophenyl boronic acid following a method similar to the one described in the synthesis of 5′-(2-methyl-biphenyl-4-ylcarbamoyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-4-carboxylic acid ethyl ester, above. The product was isolated after silica gel column purification with 20-40% EtOAc in hexanes gradient. HRMS m/z calcd for C27H28N3O3F [M+H]+: 462.2188. Found: 462.2187.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324385B2
Source datasetuspto-grants-2012_12
ORD IDord-f5bedf886de84aa29e0a410c07377119
Source noteuspto-grants-2012_12