HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706035Generated: October 27, 2026
Diisopropylamine → HCID 178494157, compound
https://huagongshe.com/reaction/706035
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 5-(2-Methoxypyrimidin-5-ylmethyl)-2-thiouracil | HCID 21936244 | — |
| Reactant | 4-(4-Fluorophenoxy)benzylchloride | HCID 22293136 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178494157 | HCID 178494157 | 55.5% |
Reaction Steps
A mixture of 5-((2-methoxypyrimidin-5-yl)methyl)-2-thioxo-2,3-dihydropyrimidin-4(1H)-one (2.75 g, 10.99 mmol), 1-(chloromethyl)-4-(4-fluorophenoxy)benzene (2.6 g, 10.99 mmol) and diisopropylamine (3.34 g, 33.0 mmol) in DCM (50 mL) was heated at 60° C. overnight. After cooling to room temperature, the mixture was washed with brine, the organic phase was dried over Na2SO4, filtered and concentrated to leave the crude product, which was slurred in EA (20 mL) for 10 min, filtered, washed with EA and concentrated in vacuo to afford the title compound (2.75 g, 51.4% yield) as white solid. LCMS: rt=1.47 min, [M+H]=451.0
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09174968B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-d0a8a9b126614314b136dacf6d02cb84 |
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| Source note | uspto-grants-2015_11 |
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