HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538922Generated: October 26, 2026
2,4,6-Trichloropyrimidine → HCID 72942068, compound
https://huagongshe.com/reaction/538922
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4,6-Trichloropyrimidine | HCID 77378 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (3S)-3-methylmorpholine | HCID 12012220 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 72942068 | HCID 72942068 | 34.2% |
Reaction Steps
The 2,4,6-trichloropyrimidine (100 mg, 053 mmol) was dissolved in dioxane (2 mL) with DIPEA (280 μL, 1.6 mmol) and (S)-3-methylmorpholine (54 mg, 0.53 mmol). The reaction mixture was heated at 130° C. under microwave irradiations for 15 min. It was then diluted with EtOAc and washed with brine. The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by preparative HPLC (Waters Sun Fire C18, 30×100 mm, 5 um; 0.1% TFA-water/acetonitrile; gradient acetonitrile 5-100% in 20 min) to afford the title compound (45 mg, 34%). tR: 3.70 min (HPLC 1); ESI-MS: 248.2/250.2 [M+H]+ (LC-MS 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865894B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-441a7cc7624c428aa34ea64df72cbb1d |
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| Source note | uspto-grants-2014_10 |
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