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2-Chloroethyl isocyanate → N-(6-Bromo-2-pyridinyl)-N'-(2-chloroethyl)urea
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Chloroethyl isocyanate | HCID 16035 | — |
| 反応物 | 2-Amino-6-bromopyridine | HCID 300809 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | N-(6-Bromo-2-pyridinyl)-N'-(2-chloroethyl)urea | HCID 58791151 | 66% |
反応手順
To a solution of 6-bromo-2-pyridinamine (1 g, 5.78 mmol) in anh. THF (25 mL), at r.t., under N2, was added 1-chloro-2-isocyanatoethane (1.2 mL, 2.5 eq) and the reaction mixture was stirred at r.t. for 18 hr. The crude mixture was partitioned between CH2Cl2 and water. The phases were separated and the organic layer was dried over anh. Na2SO4. The solids were filtered and the solvent evaporated to give the title compound (1.06 g, 66%) which was used in the next step without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07427630B2 |
| 出典データセット | uspto-grants-2008_09 |
| ORD ID | ord-a57cf86785af40228e02713709f17dc7 |
| 出典メモ | uspto-grants-2008_09 |