HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625813Generated: October 29, 2026
Ethyl 4-chloroquinazoline-2-carboxylate → HCID 86649067, compound
https://huagongshe.com/reaction/625813
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 4-chloroquinazoline-2-carboxylate | HCID 3477840 | — |
| Reactant | HCID 178420691 | HCID 178420691 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86649067 | HCID 86649067 | 37% |
Reaction Steps
A mixture of ethyl 4-chloroquinazoline-2-carboxylate (1 g, 4.2 mmol) in THF (50 mL) was filtered, and to the filtrate at −30° C. under Ar was added 0.5 M (3-chloro-4-fluorophenyl)magnesium bromide/THF (10.4 mL, 5.2 mmol). After stirring at −30° C. for 0.75 h, additional 0.5 M (3-chloro-4-fluorophenyl)magnesium bromide/THF (4.2 mL). After 1 h, the reaction was quenched by addition of saturated aq ammonium chloride and allowed to warm to rt. The mixture was extracted with EtOAc, and the extracts were dried over sodium sulfate, filtered, and concentrated under reduced pressure to afford (3-chloro-4-fluorophenyl)(4-chloroquinazolin-2-yl)methanone (495 mg, 37%) which was used directly in the next step. LC-MS (ESI) m/z 321 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09308207B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-ae067d957c7a4cf48f77d95f8d35362c |
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| Source note | uspto-grants-2016_04 |
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