Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoic Acid | HCID 243 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4-Ethoxy-2-methylamino-quinazoline-6-carbaldehyde | HCID 57590625 | — |
| Reactant | HCID 178516940 | HCID 178516940 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178467453 | HCID 178467453 | — |
Reaction Steps
To a suspension of 2-(2-chloro-4-fluoro-benzylamino)-thiazol-4-one (example 17a, 41.4 mg, 0.16 mmole), and 4-ethoxy-2-methylamino-quinazoline-6-carbaldehyde (example 12f, 45.5 mg, 0.20 mmole) in 2 mL of toluene in a microwave tube were added benzoic acid (2.0 mg, 0.016 mmole) and piperidine (1.5 mg, 0.02 mmole). The reaction mixture was heated to 150° C. with microwave for 30 min. The reaction mixture was then cooled to r.t. and the solid was filtered off, washed with toluene, MeOH and ether to give 2-(2-chloro-4-fluoro-benzylamino)-5-(4-ethoxy-2-methylamino-quinazolin-6-ylmethylene)-thiazol-4-one as a light brown solid: 46.6 mg (61.7%), MS: m/e 472 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07501428B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-2b5bde04bde24eedbe620a834e25a596 |
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| Source note | uspto-grants-2009_03 |
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