Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 216024생성일: 2026년 10월 26일
Triethylamine → 1-(5-bromo-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-N-(3-(4-fluorophenoxy)phenyl)-4-methylpiperidine-4-carboxamide
https://huagongshe.com/reaction/216024
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine | HCID 5380710 | — |
| 반응물 | N-(3-(4-fluorophenoxy)phenyl)-4-methylpiperidine-4-carboxamide | HCID 67036908 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 생성물 | 1-(5-bromo-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-N-(3-(4-fluorophenoxy)phenyl)-4-methylpiperidine-4-carboxamide | HCID 57920204 | — |
반응 단계
To a solution of N-(3-(4-fluorophenoxy)phenyl)-4-methylpiperidine-4-carboxamide from example 1, step B, (36 mg, 0.1 mmol) in isopropanol (1 mL), was added to 5-bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine from step A (24 mg, 0.1 mmol) and triethylamine (0.04 mL, 0.3 mmol). The reaction mixture was heated at 100° C. for 10 minutes under microwave condition, and then concentrated under vacuum. The product was isolated by prep HPLC to give the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08193202B2 |
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| 출처 데이터셋 | uspto-grants-2012_06 |
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| ORD ID | ord-7fa5a5f9536446e1947c6ee98c1af544 |
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| 출처 메모 | uspto-grants-2012_06 |
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