HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300074Generated: November 1, 2026
2-Iodobutane → 8-sec-Butyl-2-phenylamino-8H-pyrido[2,3-d]pyrimidin-7-one
https://huagongshe.com/reaction/2300074
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Iodobutane | HCID 10559 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-phenylamino-8H-pyrido[2,3-d]pyrimidin-7-one | HCID 10514073 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 8-sec-Butyl-2-phenylamino-8H-pyrido[2,3-d]pyrimidin-7-one | HCID 5330227 | 12% |
Reaction Steps
To a suspension of NaH (47 mg of a 60% suspension of NaH in mineral oil) in 6 mL of dimethylformamide was added 2-phenylamino-8H-pyrido[2,3-d]pyrimidin-7-one (202 mg, 0.85 mmol). The reaction mixture was heated to 50° C. to 60° C. resulting in a yellow solution. The solution was cooled slightly, and 2-iodobutane (140 μL, 1.22 mmol) was added. The reaction was heated at 50° C. for 20 minutes, then cooled to room temperature and partitioned between water and ethyl acetate. The organic layer was dried over magnesium sulfate, filtered, and concentrated in vacuo. Purification by flash chromatography eluting with 2:1 ethyl acetate:hexane gave 29 mg (12%) of 8-sec-butyl-2-phenylamino-8H-pyrido[2,3-d]pyrimidin-7-one, mp 155-156° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06498163B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-f06ff9445277496eade8ac29d9c4c1cd |
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| Source note | uspto-grants-2002_12 |
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