참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Methoxybenzaldehyde | HCID 8658 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | 6-[4-(2-Amino-ethyl)-phenoxy]-nicotinamide | HCID 59730017 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 6-{4-[2-(2-Methoxy-benzylamino)-ethyl]-phenoxy}-nicotinamide | HCID 59730396 | 85.4% |
반응 단계
Add three-angstrom molecular sieves to a stirred solution of 6-[4-(2-amino-ethyl)-phenoxy]-nicotinamide (0.1000 g, 0.3887 mmol) (compound of example 33), 2-methoxybenzaldehyde (0.047 mL, 0.39 mmol), and methanol (5 mL). Agitate the reaction for 18 h on a platform shaker at room temperature. Add sodium borohydride and agitate for 1 h at room temperature. Filter to remove the molecular sieves and load the reaction mixture directly onto a 10 g prepacked SCX cartridge. Flush with methanol (150 mL) and elute the product off the SCX cartridge with 2 M ammonia in methanol (50 mL). Concentrate on a rotary evaporator to give 0.1253 g (85%) of 6-{4-[2-(2-methoxy-benzylamino)-ethyl]-phenoxy}-nicotinamide: HPLC (30/70 to 90/10 ACN/(0.1% TFA in water) Zorbax SB-Phenyl Column 4.6 mm×15 cm×5 micron: Retention time: 4.14 minutes, Purity: 97.9%; mass spectrum (ion spray): m/z=378.1 (M+1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07560463B2 |
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| 출처 데이터셋 | uspto-grants-2009_07 |
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| ORD ID | ord-b3acef7e9e4a4039970a72a40a2eb3ff |
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| 출처 메모 | uspto-grants-2009_07 |
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