HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606380Generated: October 30, 2026
Diisopropylethylamine → HCID 178523063, compound
https://huagongshe.com/reaction/606380
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl 4-oxo-3,4-dihydroquinazoline-2-carboxylate | HCID 135437466 | — |
| Reactant | 1-(2-{[2-(1H-1,2,4-triazol-3-ylthio)ethyl]oxy}pyridin-4-yl)methanamine hydrochloride | HCID 178479186 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 178523063 | HCID 178523063 | 35% |
Reaction Steps
A suspension of ethyl 4-oxo-3,4-dihydro-2-quinazolinecarboxylate obtained according to the methods described in Journal of Organic Chemistry (1978), 43(23), 4485-7 and the like (200 mg, 0.917 mmol), 1-(2-{[2-(1H-1,2,4-triazol-3-ylthio)ethyl]oxy}pyridin-4-yl)methanamine hydrochloride obtained in Reference Example is (343 mg, 1.19 mmol) and diisopropylethylamine (462 mg, 3.57 mmol) in DMA (5 mL) was stirred at 90° C. for 15 hr. After cooling the mixture to room temperature, the resulting solid was collected by filtration, and washed with ethanol. The obtained crude powder was recrystallized from ethanol to give the title compound as a white powder (135 mg, 35%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915267B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-6a4ef7e3be68446e9e15ba8d14b4c34a |
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| Source note | uspto-grants-2011_03 |
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