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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trifluoroacetic acid → HCID 178480105, 화합물

HRID 1847984
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HRID 1847984 반응식
[CH3:1][N:2]1[CH:6]=[C:5]([C:7]2[N:8]=[CH:9][N:10](COCC[Si](C)(C)C)[CH:11]=2)[CH:4]=[N:3]1.CN1C=C(C2N(COCC[Si](C)(C)C)C=NC=2)C=N1.C(O)(C(F)(F)F)=O>C(Cl)Cl>[NH:10]1[CH:11]=[C:7]([C:5]2[CH:4]=[N:3][N:2]([CH3:1])[CH:6]=2)[N:8]=[CH:9]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6422Trifluoroacetic acidHCID 672872361-methyl-4-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-4-yl)-1H-pyrazoleHCID 866810131-methyl-4-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-5-yl)-1H-pyrazole

생성물 1

HCID 178480105HCID 178480105, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A mixture of 1-methyl-4-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-4-yl)-1H-pyrazole and 1-methyl-4-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-5-yl)-1H-pyrazole (170 mg, 0.7 mmol) from Step 2 of this Example were stirred in a 1:1 mixture of TFA and CH2Cl2 (5 mL) for 15 h. The mixture was then concentrated under reduced pressure to afford 4-(1H-imidazol-4-yl)-1-methyl-1H-pyrazole (248 mg) as an oil and was used in the next step without further purification. LCMS (ESI) m/z 149 (M+H)+.

후처리

  1. concentrationThe mixture was then concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-71da611b182d4e198d59db0cff762319
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08952058B2

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