HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989100Generated: October 25, 2026
Ammonium Chloride → 2-Chloro-4-(4-chlorophenyl)-6-cyclopropylpyrimidine
https://huagongshe.com/reaction/1989100
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Pyrimidine, 2,4-dichloro-6-(4-chlorophenyl)- | HCID 11623053 | — |
| Reactant | HCID 178420628 | HCID 178420628 | — |
| Reactant | HCID 178420684 | HCID 178420684 | — |
| Catalyst | zinc chloride THF | HCID 66790640 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Chloro-4-(4-chlorophenyl)-6-cyclopropylpyrimidine | HCID 57468616 | 42% |
Reaction Steps
To a solution of 2,4-dichloro-6-(4-chloro-phenyl)-pyrimidine (2.6 g, 10.0 mmol) and tetrakis(triphenylphosphine)palladium (0.69 g, 0.6 mmol) in THF (10 mL) was added at 20° C. a 0.25 M cyclopropylzinc chloride/THF solution (120 mL, 30 mmol; freshly prepared by stirring a mixture of 60 mL of 0.5 M cyclopropylmagnesium bromide/THF and 60 mL of 0.5 M zinc chloride/THF for 1 h at 0° C., followed by 1 h at 20° C.) and the mixture was refluxed in an atmosphere of argon for 3 h. After the slow addition of sat. aqueous NH4Cl solution (20 mL) at 0° C. the mixture was partitioned between AcOEt and 10% sodium chloride solution. The organic layer was dried (Na2SO4) and evaporated in vacuo. The residue was chromatographed on silica gel using AcOEt/cyclohexane (1:19 v/v) as eluent to give 2-chloro-4-(4-chloro-phenyl)-6-cyclopropyl-pyrimidine (1.12 g, 42%) as a light yellow solid. MS (ISP) 265.1 [(M+H)+]; mp 70-72° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07642264B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-809fb29b9f34454b8b77b38bf9a65c40 |
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| Source note | uspto-grants-2010_01 |
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