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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1802171생성일: 2026년 10월 26일

Carbon Dioxide → 4-((2-Fluoroethyl)(methyl)carbamoyl)-1-methyl-1H-pyrazole-5-carboxylic acid

https://huagongshe.com/reaction/1802171

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물PentamethyldiethylenetriamineHCID 18196—
반응물N-(2-Fluoroethyl)-N,1-dimethyl-1H-pyrazole-4-carboxamideHCID 58446960—
반응물HCID 178418306HCID 178418306—
용매TetrahydrofuranHCID 8028—
생성물4-((2-Fluoroethyl)(methyl)carbamoyl)-1-methyl-1H-pyrazole-5-carboxylic acidHCID 5844686250%

반응 조건

온도-100 °C

반응 단계

In a 50 mL three-necked flask, N-(2-fluoroethyl)-N,1-dimethyl-1H-pyrazole-4-carboxamide (500 mg, 2.7 mmol) was combined with THF (10.0 ml) to give a colorless solution. 1,1,4,7,7-Pentamethyldiethylenetriamine (621 μl, 2.97 mmol) was added, and, after cooling down to −100° C., tBuLi (1.6 M in pentane, 2.53 ml, 4.05 mmol) was added dropwise. After stirring 30 min an excess of dry ice was carefully added. After 5 min, the cooling bath was removed and the mixture was allowed to warm up to RT. H2O was added and un-reacted starting material was removed by extraction with CH2Cl2. The aqueous layer was then acidified using 1 N HCl solution, and the acid was extracted using CH2Cl2. After drying over Na2SO4, filtration and concentration in vacuum, the viscous oil was dried in HV to yield 307 mg (50%) of product as a light brown viscous oil. MS: m/z=230.2 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08349824B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-5a42e9a144ec4a7cae3dc97de1d026c4
출처 메모uspto-grants-2013_01