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Toluene → Allyl 6beta-[(allyloxycarbonyl)acetamido]-2,2-dimethylpenam-3-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Toluene | HCID 1140 | — |
| 反応物 | 6-Aminopenicillanic acid | HCID 11082 | — |
| 反応物 | Malonic acid monoallyl ester | HCID 10888030 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | Allyl 6beta-[(allyloxycarbonyl)acetamido]-2,2-dimethylpenam-3-carboxylate | HCID 67785403 | 46% |
反応手順
In a manner similar to that described for Example 1, method A, the title compound (3.53 g, 46%) was prepared from malonic acid monoallyl ester (2.88 g, 20 mmol) and 6-aminopenicillanic acid (4.33 g, 20 mmol) as colorless crystals: m.p. 59°-60° C. (toluene); IR (CHCl3) 1790, 1730, 1685 cm-1; 1 H NMR (CDCl3) δ 1.51 and 1.67 (each 3H, s, C2 -(CH3)2), 3.35-3.47 (2H, m, COCH2CO), 4.48 (1H, s, C3 -H), 4.60-4.70 (4H, m, 2xOCH2CH=CH2), 5.22-5.42 (4H, m, 2xOCH2CH=CH2), 5.56 (1H, d, J=4Hz, C5-H), 5.75 (1H, dd, J=4 and 9Hz, C6 -H), 5.84-6.00 (2H, m, 2xOCH2CH=CH2), 8.03 (1H, d, J=9Hz, NH).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05464616 |
| 出典データセット | uspto-grants-1995_11 |
| ORD ID | ord-67b89f0dcdb347d2ad2f4ceb4b51d66d |
| 出典メモ | uspto-grants-1995_11 |