HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013889Generated: October 30, 2026
HCID 178418336, compound → HCID 178418817, compound
https://huagongshe.com/reaction/1013889
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178418336 | HCID 178418336 | — |
| Reactant | HCID 178418784 | HCID 178418784 | — |
| Catalyst | HCID 178418745 | HCID 178418745 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178418817 | HCID 178418817 | — |
Reaction Steps
To a solution of the above-prepared (2-chloroquinazolin-4-yl)-(5-cyclopropyl-2H-pyrazol-3-yl)-amine (123 mg, 0.43 mmol) in THF (5 mL) is added NiCl2(dppp) (12 mg, 2.1.10−5 mol), followed by 1M benzylmagnesium chloride in THF (2.15 mL, 2.15 mmol). The solution is heated at 50° C. for 20 hours and the reaction mixture is then quenched with aqueous NH4Cl and the product extracted in ethyl acetate. The solvent is evaporated and the residue purified by flash chromatography to yield the desired (2-benzyl-quinazolin-4-yl)-(5-cyclopropyl-2H-pyrazol-3-yl)-amine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07982037B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-b70528595a534383adf6bdbc6cae26b9 |
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| Source note | uspto-grants-2011_07 |
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