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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,3-difluoro-5-iodo-N,N-dimethyl-benzamide | HCID 57975772 | — |
| Reactant | HCID 178511715 | HCID 178511715 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-fluoro-2-(4-hydroxy-cyclohexylamino)-5-iodo-N,N-dimethyl-benzamide | HCID 57975906 | 91% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07626021B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-4538d3fd61cb4d0992bb0f2ceffa5175 |
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| Source note | uspto-grants-2009_12 |
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