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Chlorophenyl isocyanate → tert-butyl 4-[N'-(2-chlorophenyl)ureido]-3-methylphenylacetate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Chlorophenyl isocyanate | HCID 76833 | — |
| 反応物 | Tert-butyl 4-amino-3-methylphenylacetate | HCID 23512173 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | tert-butyl 4-[N'-(2-chlorophenyl)ureido]-3-methylphenylacetate | HCID 23512001 | 93% |
反応手順
To a stirred mixture of tert-butyl 4-amino-3-methylphenylacetate (1.00 g, 4.52 mmol), 2-chlorophenyl isocyanate (0.55 ml, 4.52 mmol) in THF (10 ml) was added Et3 N (0.13 ml, 0.90 mmol) at room temperature. After 6 h stirring, the reaction mixture was concentrated in vacuo. The residue was triturated by the addition of n-hexane, to give tert-butyl 4-[N′-(2-chlorophenyl) ureido]-3-methylphenylacetate (1.57 g, 93%) as a pale yellow powder. mp 104–106° C. (dec.); 1H-NMR (CDCl3) δ 1.45 (s, 9H), 2.28 (s, 3H), 3.51 (s, 2H), 6.33 (br, 1H), 6.96 (t, J=7.6 Hz, 1H), 7.08 (br, 1H), 7.16–7.30 (m, 4H), 7.42 (m, 1H), 8.2 (d, J=8.1 Hz, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07179819B2 |
| 出典データセット | uspto-grants-2007_02 |
| ORD ID | ord-2e2bcdc1888c4ebda7192347bee943c6 |
| 出典メモ | uspto-grants-2007_02 |