참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Methanol--water (1/1) | HCID 22242641 | — |
| 반응물 | 2-((6-Chrysenylmethyl)amino)-2-methyl-1,3-propanediol methanesulfonate | HCID 54096087 | — |
| 생성물 | 2-((6-Chrysenylmethyl)amino)-2-methyl-1,3-propanediol 2-hydroxyethanesulfonate | HCID 131715422 | 70.4% |
반응 단계
2-((6-chrysenylmethyl)amino)-2-methyl-1,3-propanediol methanesulfonate (1C, 10.0 g, 26.63 mmol) was neutralized with 1N NaOH (30 mL) in CH3OH/H2O (200/800 mL) as in procedure 1D. The white solid which formed was filtered, washed successively with warm H2O (3×500 mL), CH3OH (200 mL), and abs. Et2O (2×500 mL), sucked semi-dry and then resuspended in CH3OH (500 mL). To this was added a 0.43M aqueous solution of 2-hydroxyethanesulfonic acid (30 mL). Slight warming gave a solution which was then filtered. The solvent was removed by rotary evaporation to give a wet white solid. This was triturated with dry Et2O, filtered, and recrystallized 3× from EtOH/Et2O to give 8.8 g (70.4%) of 2-((6-chrysenylmethyl)amino)-2-methyl-1,3-propanediol 2-hydroxyethanesulfonate, mp 212°-213°, (C, H, N, S).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04829090 |
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| 출처 데이터셋 | uspto-grants-1989_05 |
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| ORD ID | ord-8319c1b1b10a4798a5723e082b7f80df |
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| 출처 메모 | uspto-grants-1989_05 |
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