HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092664Generated: October 25, 2026
Dimethylformamide → 4-(2-Butynyloxy)-6-(4-methylpiperidino) pyrimidine
https://huagongshe.com/reaction/1092664
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Methylpiperidine | HCID 69381 | — |
| Reactant | 4-(2-Butynyloxy)-6-chloropyrimidine | HCID 12137602 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(2-Butynyloxy)-6-(4-methylpiperidino) pyrimidine | HCID 58701797 | 84.1% |
Reaction Steps
Into 2 ml of N,N-dimethylformamide was resolved 183 mg of 4-chloro-6-(2-butynyloxy)pyrimidine, 166 mg of potassium carbonate and 99 mg of 4-methylpiperidine was added therein, and the mixture was stirred for 4 hours at 80° C. The reaction mixture was cooled to near room temperature, ethyl acetate was added therein, and the mixture was washed with a saturated sodium chloride aqueous solution three times. The organic layers were dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to obtain 206 mg of 4-(2-butynyloxy)-6-(4-methylpiperidino) pyrimidine (hereinafter, referred to as Compound (18)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129526B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-bddfda6c5220488c87a71a3ba24f0f6d |
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| Source note | uspto-grants-2012_03 |
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