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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234688Generated: October 31, 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/2234688

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, 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 numberUS07709645B2
Source datasetuspto-grants-2010_05
ORD IDord-5b5f1101b3c54dcaab66ce7a6bb2229b
Source noteuspto-grants-2010_05