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Hydrogen Bromide → 1,4,5,6-Tetrahydro-5-methoxycarbonylpyrimidine Hydrobromide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrogen Bromide | HCID 260 | — |
| 反応物 | Methyl pyrimidine-5-carboxylate | HCID 253902 | — |
| 生成物 | 1,4,5,6-Tetrahydro-5-methoxycarbonylpyrimidine Hydrobromide | HCID 20080417 | 83% |
反応手順
5-Methoxycarbonylpyrimidine (1.381 g, 10 mmol) in 143 ml 0.07158M HBr was hydrogenated at 26 psig over 600 mg Pd-on-carbon 10% in a Parr hydrogenator for three hours. The suspension was filtered and the filter rinsed twice with hot water (10 ml). The filtrate was evaporated in vacuo to give 1.86 g yellow oil (83%). The oil was crystallized from anhydrous ethanol/THF, and the hygroscopic crystals collected by decanting the solvents under a stream of nitrogen. Excess solvents were removed under vacuum in a drying pistol to yield 1.01 g (45%) white crystals mp 149°-153° C. (with the evolution of gas). Microanalysis calc.: C32.3, H 4.97, N 12.56; found: C 32.12, H 5.15, N 12.34. MHz nmr indicated product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05403845 |
| 出典データセット | uspto-grants-1995_04 |
| ORD ID | ord-8ab72d8812054e6b9d89551e21f4712d |
| 出典メモ | uspto-grants-1995_04 |