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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1930339생성일: 2026년 10월 27일

Hydrochloric Acid → 2,2,2-Trichloroethyl 1-isopropyl-3-(thiophen-2-yl)-1h-pyrazol-5-ylcarbamate

https://huagongshe.com/reaction/1930339

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TriethylamineHCID 8471—
반응물1,1,2-TrichloroethanolHCID 119427—
반응물P,P-Diphenylphosphinic azideHCID 199401—
반응물1-isopropyl-3-(thiophen-2-yl)-1H-pyrazole-5-carboxylic acidHCID 69035933—
용매1,4-DioxaneHCID 31275—
생성물2,2,2-Trichloroethyl 1-isopropyl-3-(thiophen-2-yl)-1h-pyrazol-5-ylcarbamateHCID 6903648480%

반응 조건

온도90 °C

반응 단계

To a solution of 1-isopropyl-3-(thiophen-2-yl)-1H-pyrazole-5-carboxylic acid (0.68 g, 2.9 mmol) in dioxane (10 mL) was added with triethylamine (0.44 g, 4.3 mmol), diphenylphosphorylazide (0.95 g, 3.5 mmol) and trichloroethanol (0.86 g, 5.8 mmol) and the mixture was heated to 90° C. for 4 h. The mixture was poured into 3 M HCl (40 mL) solution and the product was extracted with EtOAc (2×40 mL). The combined organics were washed with brine, dried (Na2SO4) and concentrated in vacuo. Purification by silica gel chromatography provided 2,2,2-trichloroethyl 1-isopropyl-3-(thiophen-2-yl)-1H-pyrazol-5-ylcarbamate (0.88 g, 80% yield) as a white solid. 1H NMR (400 MHz, Acetone-d6): δ 7.36-7.34 (m, 3H), 7.07 (dd, J=5.6 Hz, 4.0 Hz, 1H), 6.52 (s, 1H), 5.83 (t, J=7.2 Hz, 3H), 4.95 (s, 2H), 4.66-4.62 (m, 1H), 1.45 (d, J=6.8 Hz, 6H); MS (ESI) m/z: 382.0 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08188113B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-c0c9cca43ad8428dbf78179843149592
출처 메모uspto-grants-2012_05