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HRID 2109720作成日:2026年10月25日
Cesium carbonate → N-((S)-2-amino-3-(4-(trifluoromethyl)phenyl)propyl)-5-(phthalazin-6-yl)thiazol-2-amine
https://huagongshe.com/reaction/2109720
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Mercapto-ethanol | HCID 4713212 | — |
| 反応物 | Tert-butyl 5-(phthalazin-6-yl)thiazol-2-ylcarbamate | HCID 57633940 | — |
| 反応物 | 4-(Trifluoromethyl)benzyl-1-(4-nitrophenylsulfonyl)aziridine | HCID 76571302 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | N-((S)-2-amino-3-(4-(trifluoromethyl)phenyl)propyl)-5-(phthalazin-6-yl)thiazol-2-amine | HCID 23654432 | 19% |
反応手順
A solution of tert-butyl 5-(phthalazin-6-yl)thiazol-2-ylcarbamate (0.320 g, 0.97 mmol) and Cs2CO3 (0.63 g, 1.9 mmol) in DMF was stirred at room temperature for 30 minutes. The resulting solution was treated dropwise with ((S)-2-(4-(trifluoromethyl)benzyl-1-(4-nitrophenylsulfonyl)aziridine in DMF, and was then stirred for 30 minutes. The reaction was treated in portions with K2CO3 (0.67 g, 4.9 mmol) and mercaptoethanol (0.23 g, 2.9 mmol) and stirred for 15 minutes. After removing the solvent under reduced pressure, the residue was adsorbed onto a plug of silica gel and chromatographed through a Redi-Sep pre-packed silica gel column (40 g), eluting with a gradient of 5% to 95% MeOH in DCM. The resulting residue was dissolved in DCM and treated with TFA to provide the title compound (0.100 g, 19% yield). LCMS (M+H+) 430.6 calc. for C21H18F3N5S 430.6; 1H NMR (400 MHz, CDCl3-d) δ ppm 9.48 (s, 1H), 9.44 (s, 1H), 8.01 (d, 1H), 7.92 (d, 1H), 7.75 (s, 1H), 7.62 (sd, 3H), 7.35 (d, 2H), 3.92 (dd, 2H), 3.55 (dd, 1H), 3.25 (tt, 1H) 2.98 (dd, 1H), 2.89 (t, 2H), 2.72 (b, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07514566B2 |
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| 出典データセット | uspto-grants-2009_04 |
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| ORD ID | ord-eebd43348ba04881a676e70afaa1bd94 |
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| 出典メモ | uspto-grants-2009_04 |
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