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(2-Methoxyethyl)(methyl)amine → 3-Chloro-5-[(7-{(2E)-4-[(2-methoxyethyl)(methyl)amino]but-2-enoyl}-5,6,7,8-tetrahydropyrido[4',3':4,5]thieno[2,3-d]pyrimidin-4-yl)amino]phenol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (2-Methoxyethyl)(methyl)amine | HCID 300977 | — |
| 反応物 | 4-Bromocrotonic acid | HCID 6436411 | — |
| 反応物 | 3-Chloro-5-(5,6,7,8-tetrahydropyrido[4',3':4,5]thieno[2,3-d]pyrimidin-4-ylamino)phenol hydrochloride | HCID 66850088 | — |
| 生成物 | 3-Chloro-5-[(7-{(2E)-4-[(2-methoxyethyl)(methyl)amino]but-2-enoyl}-5,6,7,8-tetrahydropyrido[4',3':4,5]thieno[2,3-d]pyrimidin-4-yl)amino]phenol | HCID 58116832 | — |
反応手順
In analogy to Example 130, the title compound was prepared from (2E)-4-bromobut-2-enoic acid (84 mg, 0.41 mmol), 3-chloro-5-(5,6,7,8-tetrahydropyrido[4′,3′:4,5]thieno[2,3-d]pyrimidin-4-ylamino)phenol hydrochloride from Example 65A (100 mg, 0.27 mmol) and 2-methoxy-N-methylethanamine (39 mg, 0.43 mmol) to yield 24 mg (18%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08524722B2 |
| 出典データセット | uspto-grants-2013_09 |
| ORD ID | ord-d0e5a0a39b6b4fec96b7029fa3cc18b4 |
| 出典メモ | uspto-grants-2013_09 |