Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 423561생성일: 2026년 10월 25일
Sodium Carbonate → 1-Methylethyl 4-({[6-(4-{[(2-hydroxyethyl)amino]sulfonyl}phenyl)-3-pyridinyl]oxy}methyl)-1-piperidinecarboxylate
https://huagongshe.com/reaction/423561
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | (4-(N-(2-Hydroxyethyl)sulfamoyl)phenyl)boronic acid | HCID 44119332 | — |
| 반응물 | HCID 86638737 | HCID 86638737 | — |
| 촉매 | HCID 178418476 | HCID 178418476 | — |
| 용매 | 1,2-Dimethoxyethane | HCID 8071 | — |
| 생성물 | 1-Methylethyl 4-({[6-(4-{[(2-hydroxyethyl)amino]sulfonyl}phenyl)-3-pyridinyl]oxy}methyl)-1-piperidinecarboxylate | HCID 24992753 | 27% |
반응 단계
The title compound (70 mg, 27%) was prepared as a white solid from (4-{[(2-hydroxyethyl)amino]sulfonyl}phenyl)boronic acid (130 mg, 0.55 mmol), 1-methylethyl 4-{[(6-bromo-3-pyridinyl)oxy]methyl}-1-piperidinecarboxylate (prepared as in Example 81, Step 1, 197 mg, 0.55 mmol), Pd(PPh3)2Cl2 (100 mg, 0.14 mmol), 2M Na2CO3 (2 mL) and DME (4 mL) in a manner similar to Example 21, Step 3. 1H NMR (400 MHz, CDCl3): δ 8.36 (d, 1H, J=2.9 Hz), 8.05 (d, 2H, J=8.6 Hz), 7.91 (d, 2H, J=8.6 Hz), 7.69 (d, 1H, J=8.8 Hz), 7.26 (dd, 1H, Ja=8.8 Hz, Jb=2.9 Hz), 5.11 (t, 1H, J=6.0 Hz), 4.96-4.83 (m, 1H), 4.20 (bs, 2H), 3.89 (d, 2H, J=6.2 Hz), 3.70-3.61 (m, 2H), 3.13-2.99 (m, 2H), 2.83-2.70 (m, 2H), 2.07-1.92 (m, 1H), 1.89-1.79 (m, 2H), 1.70 (bs, 1H), 1.37-1.17 (m, 8H); LRMS (ESI), m/z 478 (M+H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08101634B2 |
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| 출처 데이터셋 | uspto-grants-2012_01 |
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| ORD ID | ord-a5f4b26ff8dc4aadb7b027755a2bad53 |
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| 출처 메모 | uspto-grants-2012_01 |
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