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HRID 535429作成日:2026年10月25日
Dicyclohexylcarbodiimide → 2-(methylamino)-N-[6-(2-phenylethynyl)-4-(trifluoromethyl)pyridin-2-yl]propanamide
https://huagongshe.com/reaction/535429
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 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-(2-Phenylethynyl)-4-(trifluoromethyl)pyridin-2-amine | HCID 86694420 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 生成物 | 2-(methylamino)-N-[6-(2-phenylethynyl)-4-(trifluoromethyl)pyridin-2-yl]propanamide | HCID 71714918 | — |
反応手順
A mixture of 2-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]propanoic acid (620 mg, 3.05 mmol) and N,N′-dicyclohexylcarbodiimide (315 mg, 1.53 mmol) in DCM (4 ml) is stirred at RT for 30 minutes. This mixture is added to 6-(2-phenylethynyl)-4-(trifluoromethyl)pyridin-2-amine B3b (100 mg, 0.38 mmol) and DIPEA (73 μl; 0.42 mmol) in NMP (5 ml). After stirring for 6 days at 50° C. the reaction mixture is concentrated in vacuo and the boc-protected product purified by NP chromatography. The boc-protected product is treated with DCM:TFA (9:1, 4 ml) for 1.5 h at RT. This mixture is diluted with DCM and extracted with a saturated aqueous solution of NaHCO3. The combined organic layers are dried over MgSO4 and concentrated in vacuo. The product is purified by RP HPLC. Yield: 10.2 mg (8%). HPLC-MS: M+H=348; tR=1.46 (*Method—1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08859541B2 |
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| 出典データセット | uspto-grants-2014_10 |
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| ORD ID | ord-515122b4d2094f3b84f0b55beec6f044 |
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| 出典メモ | uspto-grants-2014_10 |
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