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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865675Generated: October 28, 2026

2,3-difluoro-5-iodo-N,N-dimethyl-benzamide → 3-fluoro-2-(4-hydroxy-cyclohexylamino)-5-iodo-N,N-dimethyl-benzamide

https://huagongshe.com/reaction/1865675

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-difluoro-5-iodo-N,N-dimethyl-benzamideHCID 57975772—
ReactantHCID 178511715HCID 178511715—
SolventHydrochloric AcidHCID 313—
SolventDichloromethaneHCID 6344—
Product3-fluoro-2-(4-hydroxy-cyclohexylamino)-5-iodo-N,N-dimethyl-benzamideHCID 5797590691%

Reaction Steps

2,3-Difluoro-5-iodo-N,N-dimethyl-benzamide (2.36 g, 7.6 mmol) and trans-4-amino-cyclohexanol (3.5 g, 30 mmol) were stirred at 120° C. for 5 hrs. The resulting solid was dissolved in 1 N hydrochloric acid and dichloromethane. The aqueous layer was extracted with dichloromethane twice. The combined organic phases were washed with saturated aqueous sodium bicarbonate solution and brine, dried over magnesium sulfate and concentrated to give 2.8 g (6.84 mmol, 91%) of 3-fluoro-2-(4-hydroxy-cyclohexylamino)-5-iodo-N,N-dimethyl-benzamide as a white solid. 1H NMR (500 MHz, DMSO-d6) δ 7.45 (dd, J=12 Hz, J2=2 Hz, 1H), 7.15 (s, 1H), 4.57 (dd, J=10 Hz, J2=3 Hz, 1H), 4.50 (d, J=4.5 Hz, 1H), 3.33 (m, 1H), 3.02 (m, 1H), 2.94 (bs, 3H), 2.81 (bs, 3H), 1.74 (m, 4H), 1.04-1.24 (m, 4H); MS: m/z 407 [MH+]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07626021B2
Source datasetuspto-grants-2009_12
ORD IDord-4538d3fd61cb4d0992bb0f2ceffa5175
Source noteuspto-grants-2009_12