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Dicyclohexylcarbodiimide → tert-butyl-N-methyl-N-(1-{[6-(2-phenylethynyl)-4-(pyridin-4-yl)pyridin-2-yl]-carbamoyl}ethyl)carbamate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 2-(((Tert-butoxy)carbonyl)(methyl)amino)propanoic acid | HCID 4436857 | — |
| 反応物 | 6-(Phenylethynyl)-[4,4'-bipyridin]-2-amine | HCID 117911001 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 生成物 | tert-butyl-N-methyl-N-(1-{[6-(2-phenylethynyl)-4-(pyridin-4-yl)pyridin-2-yl]-carbamoyl}ethyl)carbamate | HCID 117903139 | — |
反応手順
A mixture of 2-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]propanoic acid (1.44 g, 7.1 mmol) and N,N′-dicyclohexylcarbodiimide (0.73 g, 3.55 mmol) in DCM (4 ml) is stirred for 30 minutes at RT. This mixture is added in 4 portions over 48 h via syringe filter to a mixture of 6-(2-phenylethynyl)-4-(pyridin-4-yl)pyridin-2-amine G1 (0.24 g, 0.89 mmol), DIPEA (166 μl, 0.98 mmol) and NMP (2 ml) at 50° C. After stirring for another 16 h at 50° C. the mixture is filtered and the product purified by RP HPLC. Yield: 56 mg (14%). HPLC-MS: M+H=457; tR=.2.08 min (METHOD—2).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09278978B2 |
| 出典データセット | uspto-grants-2016_03 |
| ORD ID | ord-24de4df4926842b28a6435c149caebc5 |
| 出典メモ | uspto-grants-2016_03 |