関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Cenisertib | HCID 11569967 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 2,4-Diaminopyrimidine | HCID 67431 | — |
| 生成物 | Ammonia methanol | HCID 21705897 | 2% |
反応手順
A sealed tube charged with enantiomerically pure mono-SNAr product 57a (2.25 g, 8 mmol), aniline 7 (1.80 g, 8.8 mmol), TEA (1.12 mL) and methanol (18 mL) was stirred at 100° C. for 24 hours. The resulting viscous but homogeneous solution was concentrated and the residue was chromatographed (silica gel, CH2Cl2 then 2-5% 2N NH3/MeOH in CH2Cl2) to afford the expected 2,4-diaminopyrimidine derivative 60a (2.28 g, 63%; purity: 95% AUC; enantiomeric purity; greater than 99% as determined by chiral HPLC. The chiral analytical data, 1H NMR and LCMS analyses were found to be identical with the enantiomer designated E1; [α]DRI+44.4° (c 1.0, MeOH).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07868013B2 |
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| 出典データセット | uspto-grants-2011_01 |
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| ORD ID | ord-0085a8e6da25410ab46fc77e86ab5e2a |
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| 出典メモ | uspto-grants-2011_01 |
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