HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070951Generated: October 25, 2026
4-Amino-3,5-dichlorobenzotrifluoride → 4-[[4-[2,6-Dichloro-4-(trifluoromethyl)anilino]pyrimidin-2-yl]amino]benzonitrile
https://huagongshe.com/reaction/1070951
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Amino-3,5-dichlorobenzotrifluoride | HCID 141094 | — |
| Reactant | 2-[(4-Cyanophenyl)amino]4-pyrimidinyl trifluoromethanesulfonate | HCID 22398451 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-[[4-[2,6-Dichloro-4-(trifluoromethyl)anilino]pyrimidin-2-yl]amino]benzonitrile | HCID 488774 | 9.2% |
Reaction Steps
2-[(4-cyanophenyl)amino]-4-pyrimidinyl trifluoromethanesulfonate (0.0022 mol) and 2,6-dichloro-4-(trifluoromethyl)-benzenamine (0.0044 mol) were combined in 1,4-dioxane (2.5 ml) and heated in a sealed tube under Ar at 170° C. for 40 hours. The reaction mixture was allowed to cool to room temperature. Silica gel was added, and the solvent was evaporated. The residue was purified by flash column chromatography over silica gel (eluent gradient: CH2Cl2:CH3OH:NH4OH 100:0:0 to 97:2.7:0.3). The desired fractions were collected and the solvent was evaporated. The residue was recrystallized from CH3CN, filtered off and dried, yielding 0.086 g (9.2%) of 4-[[4-[[2,6-dichloro-4-(trifluoromethyl)-phenyl]amino]-2-pyrimidinyl]amino]benzonitrile (compound 66).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06903213B2 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-bd145d35e4714fe8bb3911bb5818d553 |
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| Source note | uspto-grants-2005_06 |
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