Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 897960생성일: 2026년 10월 25일
Trifluoroacetic acid methylene chloride → 3-(4-amino-3-methoxyphenyl)-1-(1-methyl-4-piperidyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine
https://huagongshe.com/reaction/897960
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Trifluoroacetic acid methylene chloride | HCID 21863450 | — |
| 반응물 | tert-butyl N-{4-[4-amino-1-(1-methyl-4-piperidyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-2-methoxyphenyl}carbamate | HCID 22347171 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 3-(4-amino-3-methoxyphenyl)-1-(1-methyl-4-piperidyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine | HCID 22347016 | 95.2% |
반응 단계
A mixture of trifluoroacetic acid/dichloromethane (20:80, 7 mL) was added to a solution of tert-butyl N-{4-[4-amino-1-(1-methyl-4-piperidyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-2-methoxyphenyl}carbamate (240 mg, 0.529 mmol) in dichloromethane (4 mL) at 0° C. 15 minutes later, the ice-bath was removed and the reaction mixture was stirred at room temperature for 4 hours. The solvents were evaporated and the residue was dissolved in dichloromethane. Sodium hydroxide (1.0N) was added to adjust the pH to about 10. The layers were separated and the aqueous layer was extracted with dichloromethane four times. The combined organic layer was washed with brine, dried over MgSO4, filtered and evaporated to give 3-(4-amino-3-methoxyphenyl)-1-(1-methyl-4-piperidyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (178 mg, 95%). HPLC (Waters 486-Column: delta pak, C18, 5 um, 300 Å, 150×3.9 mm. Eluents: 5% B/A to 95% B/A in 10 min. (B: acetonitrile, A: 50 mM ammonia acetate buffer, pH 4.5), 1.0 mL/min.) Rt=6.45 min.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06921763B2 |
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| 출처 데이터셋 | uspto-grants-2005_07 |
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| ORD ID | ord-b60c97f5e9754088abd5db707462823c |
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| 출처 메모 | uspto-grants-2005_07 |
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