HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 60428Generated: October 28, 2026
5-((4-chlorophenyl)(hydroxy)methyl)-6-((5-chloropyridin-3-yl)oxy)-1-methyl-3-(3-((tetrahydro-2H-pyran-2-yl)oxy)propyl)pyrido[2,3-d]pyrimidine-2,4 (1H,3H)-dione → HCID 118875885, compound
https://huagongshe.com/reaction/60428
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-((4-chlorophenyl)(hydroxy)methyl)-6-((5-chloropyridin-3-yl)oxy)-1-methyl-3-(3-((tetrahydro-2H-pyran-2-yl)oxy)propyl)pyrido[2,3-d]pyrimidine-2,4 (1H,3H)-dione | HCID 118875527 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | HCID 118875885 | HCID 118875885 | 38% |
Reaction Steps
To a solution of 5-((4-chlorophenyl)(hydroxy)methyl)-6-((5-chloropyridin-3-yl)oxy)-1-methyl-3-(3-((tetrahydro-2H-pyran-2-yl)oxy)propyl)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione (120 mg, 0.204 mmol) in HCOOH (5 mL) was added Zn dust (66.8 mg, 1.02 mmol). The reaction was heated at 70° C. for 1.5 h, cooled to RT and filtered. The filtrate was concentrated to give 3-(5-(4-chlorobenzyl)-6-((5-chloropyridin-3-yl)oxy)-1-methyl-2,4-dioxo-1,2-dihydropyrido[2,3-d]pyrimidin-3(4H)-yl)propyl formate (40 mg, 38.0% yield) as an oil. LCMS MH+ 515 and TR=1.696 min. Used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09440972B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-6a9d9b3e2ab9496bb2a50000973d4498 |
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| Source note | uspto-grants-2016_09 |
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