関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Phosgene | HCID 6371 | — |
| 反応物 | Sulphonyl diisocyanate | HCID 77898 | — |
| 反応物 | 2-Amino-4,6-dimethoxypyrimidine | HCID 118946 | — |
| 反応物 | 2-(Chloromethyl)-N-(butylaminocarbonyl)benzenesulfonamide | HCID 13631887 | — |
| 反応物 | 2-(Chloromethyl)benzenesulfonyl isocyanate | HCID 20152699 | — |
| 触媒 | Diazabicyclo(2.2.2)octane | HCID 136165 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 生成物 | 2-(Chloromethyl)-N-[(4,6-dimethoxypyrimidin-2-yl)-aminocarbonyl]benzenesulfonamide | HCID 13364617 | 69.6% |
反応手順
A solution of 2-(chloromethyl)-N-(butylaminocarbonyl)benzene sulfonamide (1.33 g, 4.38 mmol) and diazabicyclo[2.2.2]octane (5 mg) in xylene (12 ml) was heated at reflux and contacted in portions with phosgene (1.0 ml. condensed phase). After 2.0 hrs at reflux, the mixture was cooled to room temperature, decanted, and volatiles were removed to give 1.56 g of crude product. The IR spectrum of 2-(chloromethyl)benzenesulfonyl isocyanate featured a strong band at 2250 cm-1. The crude sulfonyl isocyanate was contacted with acetonitrile (10 ml) and 2-amino-4,6-dimethoxypyrimidine (0.68 g, 4.4 mmol) and stirred for 16 hrs. Filtration gave 1.18 g of white solid, mp 192°-193°. The sample was dissolved in 0.5N NaOH, filtered and pH adjusted to 6.5. The mixture was cooled and filtered and the solid washed with ice water and dried to give 0.90 g of white solid. 1H nmr δDMSO-d6TMS 12.7 (brd s, 10.50 (s, 1H) 8.13-7.97 (m, 1H), 7.73-7.40 (m, 3H), 5.90 (s, 1H), 5.10 (s, 2H), 3.87 (s, 6H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US04723990 |
|---|
| 出典データセット | uspto-grants-1988_02 |
|---|
| ORD ID | ord-7101f12d796b4a7697ca6546a96de61b |
|---|
| 出典メモ | uspto-grants-1988_02 |
|---|