Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Zinc | HCID 23994 | — |
| Reactant | 4-Chloro-2-phenylquinazoline | HCID 80977 | — |
| Reactant | Methyl 4-(bromomethyl)(1,1'-biphenyl)-2-carboxylate | HCID 19595328 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178497614 | HCID 178497614 | — |
Reaction Steps
[[2'-(methoxycarbonyl)(1,1'-biphenyl)-4-yl]-methyl]zinc bromide was prepared in advance from 400 mg of zinc in 1 ml of tetrahydrofuran and 1.53 g of methyl 4-(bromomethyl)(1,1'-biphenyl)-2-carboxylate (KNOCHEL, J. Org. Chem., 1988, Vo. 53, p. 5789 to 5791) and 240.69 mg of 4-chloro-2-phenyl-quinazoline and 115 mg of palladium tetrakis(triphenyl-phosphine) complex were added to the solution. The mixture stood at 50° C. for 6 hours and the reaction medium was poured into a water/ice/acetic acid mixture. The aqueous phase was extracted with ethyl acetate and the organic phase was washed with water and water saturated with sodium chloride, dried and evaporated. After chromatography on silica (eluant:ethyl acetate-hexane 1-9 then 2-8), 260 mg of expected product melting at 120° C. to 121° C. after crystallization from isopropyl ether were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05817674 |
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| Source dataset | uspto-grants-1998_10 |
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| ORD ID | ord-27047be21b884980abc838eabf5dd9ae |
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| Source note | uspto-grants-1998_10 |
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