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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389012Generated: October 30, 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/2389012

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, J1=12 Hz, J2=2 Hz, 1H), 7.15 (s, 1H), 4.57 (dd, J1=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 numberUS08268994B2
Source datasetuspto-grants-2012_09
ORD IDord-fbd1cd5b53604a4fa9c8a2282480655a
Source noteuspto-grants-2012_09