HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461707Generated: October 25, 2026
Piperazine → 5-Methoxy-4-(piperazin-1-yl)pyrimidine
https://huagongshe.com/reaction/1461707
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 4,6-Dichloro-5-methoxypyrimidine | HCID 78720 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Methoxy-4-(piperazin-1-yl)pyrimidine | HCID 10420152 | — |
Reaction Steps
Piperazine (20 g) was dissolved in water (100 mL) in a Parr bottle and then solid 4,6-dichloro-5-methoxypyrimidine (5.00 g, 27.9 mmol) was added. The mixture was vigorously stirred for 2 h at room temperature during which the 4,6-dichloro-5-methoxypyrimidine dissolved. The stirring bar was removed, catalyst (10% Pd/C, 1.0 g) was added to the turbid solution, and the mixture was then hydrogenated (60 psi, 3 h) at room temperature. The catalyst was filtered off and the filtrate extracted 3 times with CH2Cl2. The CH2Cl2 extracts were dried over Na2SO4 and concentrated in vacuo to give a clear oil which solidified upon standing (3.34 g, 61.7%). This crude product was Kugelrohr distilled (yield 3.24 g), dissolved in acetonitrile, and concentrated HCl added to precipitate the product as a white powder which was dried in vacuo (4.32 g, 94.0% from crude product, m.p. 219°-221.5° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05077293 |
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| Source dataset | uspto-grants-1991_12 |
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| ORD ID | ord-1ee9ad182cba4bab81fb112817408ace |
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| Source note | uspto-grants-1991_12 |
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