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Acetone, oxime → 7a-(3-methyl-5-isoxazolyl)-hexahydro-1H-pyrrolizine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetone, oxime | HCID 67180 | — |
| 反応物 | Methyl hexahydro-1H-pyrrolizine-7a-carboxylate | HCID 394149 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 生成物 | 7a-(3-methyl-5-isoxazolyl)-hexahydro-1H-pyrrolizine | HCID 18934742 | 11.2% |
反応手順
8-(Methoxycarbonyl)-hexahydro-1H-pyrrolizine (from step 1d, 1.56 g, 9.22 mmol), acetone oxime (1.45 g, 19.8 mmol) and n-butyllithium (2.5M in hexane, 16 mL, 39.6 mmol) were combined in a similar fashion as that outlined by J. Saunders et at., J. Med. Chem. 1990, 33: 1128. The crude material was chromatographed (silica gel; CHCl3 /MeOH, 99:1) to afford a yellow oil (199 mg, 11%). MS (CI/NH3) m/e: 193 (M+H)+. 1H NMR (CDCl3, 300 MHz) δ1.76-1.92 (m, 6H), 2.14-2.29 (m, 2H), 2.24 (s, 3H), 2.61-2.69 (m, 2H), 3.13-3.32 (m, 2H), 5.95 (s, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05733912 |
| 出典データセット | uspto-grants-1998_03 |
| ORD ID | ord-0a13f316069a49f782b0a73c4007b4d6 |
| 出典メモ | uspto-grants-1998_03 |