HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375478Generated: October 31, 2026
3,4-Dichloroaniline → HCID 10226296, compound
https://huagongshe.com/reaction/2375478
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-Dichloroaniline | HCID 7257 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | HCID 21101361 | HCID 21101361 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 10226296 | HCID 10226296 | 65.8% |
Reaction Steps
Potassium tert-butoxide (1.6 mmol, 1 M in 2-methyl 2-propanol) was added to a solution of N-[2-(4-benzyl-1-piperazinyl)-6-chloro-4-pyrimidinyl]-N,N-dimethylamine (0.331 g, 0.997 mmol) and 3,4 dichloroaniline (0.178 g, 1.10 mmol) in dioxane (2 mL). Subsequently, tris(dibenzylidineacetone)dipalladium (40 mg, 0.04 mmol) and 2,2′-Bis(diphenylphosphino)-1,1′-binapthyl (44 mg, 0.070 mmol) were added and the mixture was stirred for 7 h at 110° C. The resulting mixture was cooled to room temperature and concentrated under reduced pressure. The residue was treated with saturated NaHCO3 (50 mL) and extracted with CH2Cl2 (3×50 mL). The organic layer washed with brine (2×100 mL), dried over Na2SO4, concentrated in vacuo, and purified by preparative TLC using hexane/EtOAc to give the desired product (300 mg, 65%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07465750B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-0e17b5d5d1094a428ba5460323ec4ffd |
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| Source note | uspto-grants-2008_12 |
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