참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Acetaldehyde | HCID 177 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 반응물 | 2-(Mesitylmethyl)-1-methyl-1H-benzimidazol-7-amine | HCID 59202092 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | N,N-Diethyl-2-(mesitylmethyl)-1-methyl-1H-benzimidazol-7-amine | HCID 24851690 | 98.6% |
반응 단계
To a solution of 2-(mesitylmethyl)-1-methyl-1H-benzimidazol-7-amine (200 mg, 0.717 mmol), acetaldehyde (0.400 mL, 7.17 mmol) and acetic acid (0.330 mL, 5.78 mmol) in methanol (5.0 mL) was added sodium triacetoxyborohydride (1.52 g, 7.17 mmol) portionwise at 0° C. The mixture was warmed to room temperature and stirred for 14 hr. Saturated aqueous sodium bicarbonate solution (50 mL) was added to the mixture and the mixture was extracted with ethyl acetate (25 mL, three times). Combined organic layers were washed with saturated aqueous sodium bicarbonate solution (20 mL) and brine, dried over anhydrous sodium sulfate and concentrated in vacuo to afford the title compound (237 mg, 0.707 mmol, 97%) as a colorless solid. The resulting solid was recrystallized from n-hexane/ethyl acetate to give the title compound (145 mg, 0.433 mmol).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08039500B2 |
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| 출처 데이터셋 | uspto-grants-2011_10 |
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| ORD ID | ord-d4c2877530d54b2d8b6c87fb51b4651e |
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| 출처 메모 | uspto-grants-2011_10 |
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