Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1922809생성일: 2026년 10월 26일
Acetic Acid → 1-[2-(2-Chloro-9-methyl-6-morpholin-4-yl-9H-purin-8-yl)ethyl]-4-methylpiperidin-4-ol
https://huagongshe.com/reaction/1922809
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Trimethyl orthoformate | HCID 9005 | — |
| 반응물 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 반응물 | 4-Methylpiperidin-4-ol | HCID 15649174 | — |
| 반응물 | (2-chloro-9-methyl-6-morpholin-4-yl-9H-purin-8-yl)acetaldehyde | HCID 59605819 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 생성물 | 1-[2-(2-Chloro-9-methyl-6-morpholin-4-yl-9H-purin-8-yl)ethyl]-4-methylpiperidin-4-ol | HCID 59605907 | 17% |
반응 단계
To a solution of (2-chloro-9-methyl-6-morpholin-4-yl-9H-purin-8-yl)acetaldehyde (200 mg, 0.68 mmol) in DCE (15 mL) was added 4-methylpiperidin-4-ol (117 mg, 1.01 mmol), trimethyl orthoformate (0.74 mL, 6.76 mmol) and acetic acid (0.04 mL, 0.68 mmol). The reaction mixture was stirred at room temperature for 1.5 h, sodium triacetoxyborohydride (187 mg, 1.35 mmol) was added and the resulting mixture stirred for a further 18 h. The reaction mixture was loaded onto an Isolute® SCX-2 cartridge, washed with MeOH then the desired product eluted with 2 M NH3/MeOH in DCM. The resulting residue was purified by column chromatography (Si—PCC, 0-20% 2 M NH3/MeOH in DCM) to give the title compound as a colourless oil (45 mg, 17%). LCMS (Method H): RT=2.24 min, [M+H]+ 395.5
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08173650B2 |
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| 출처 데이터셋 | uspto-grants-2012_05 |
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| ORD ID | ord-cd493ad662aa4d998c0c83042c245a9f |
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| 출처 메모 | uspto-grants-2012_05 |
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