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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672938Generated: October 31, 2026

3,4-Difluoro-2-(2-fluoro-4-iodoanilino)benzoyl fluoride → HCID 59469195, compound

https://huagongshe.com/reaction/1672938

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Difluoro-2-(2-fluoro-4-iodoanilino)benzoyl fluorideHCID 59469158—
ReactantHCID 67051825HCID 67051825—
ProductHCID 59469195HCID 59469195—

Reaction Steps

The compounds of examples 25a and 25b were synthesized starting from benzyl 3-hydroxy-3-(2-oxycyclohenyl)azetidine-1-carboxylate prepared according to the procedure given in example 25. The ketone was reduced to give benzyl 3-hydroxy-3-(2-hydroxycyclohexyl)azetidine-1-carboxylate as a mixture of racemic diastereomers which were subjected to hydrogenation to afford 3-(2-hydroxycyclohexyl)azetidin-3-ol. 3-(2-hydroxycyclohexyl)azetidin-3-ol was then carried forward in a coupling step with 3,4-difluoro-2-(2-fluoro-4-iodophenylamino)benzoyl fluoride in the usual manner. The coupled material thus obtained was purified by preparative reverse phase HPLC where fraction 1 was tentatively assigned as (±)-1-({3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}carbonyl)-3-[(trans)-2-hydroxycyclohexyl]azetidin-3-ol (Example 25a) and fraction 2 was tentatively assigned as (±)-1-({3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}carbonyl)-3-[(cis)-2-hydroxycyclohexyl]azetidin-3-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07999006B2
Source datasetuspto-grants-2011_08
ORD IDord-ea39b169c9f344d09bde250e4e002bc4
Source noteuspto-grants-2011_08