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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2196497생성일: 2026년 10월 26일

Hydrochloric Acid → (S)-tert-butyl 1-((4-(5-(furan-2-yl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)thiophen-2-yl)methylamino)-1-oxopropan-2-ylcarbamate

https://huagongshe.com/reaction/2196497

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TriethylamineHCID 8471—
반응물Boc-Ala-OSuHCID 11011585—
반응물(4-(5-(furan-2-yl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)thiophen-2-yl)methanamineHCID 59843286—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물(S)-tert-butyl 1-((4-(5-(furan-2-yl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)thiophen-2-yl)methylamino)-1-oxopropan-2-ylcarbamateHCID 5984320149%

반응 단계

(S)-2,5-Dioxopyrrolidin-1-yl 2-(tert-butoxycarbonylamino)propanoate (130 mg, 0.45 mmol) was added to amine 5 (110 mg, 0.35 mmol) and Et3N (94.4 mg, 130 μL, 0.93 mmol) in DCM (2 mL) and DMF (0.2 mL) and the mixture was stirred at room temperature for 36 h. DCM was added followed by 1N HCl and the organic layer was separated and washed with H2O, then with saturated NaHCO3, dried over MgSO4, filtered and concentrated. The crude material was purified by chromatography (Biotage, 25+S column) eluting with 0-50% EtOAc/hexanes. Compound 6 was obtained in 49% yield as a white solid. LRMS (ESI): calc. 484.5; found 507.1 (MNa)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08338437B2
출처 데이터셋uspto-grants-2012_12
ORD IDord-7324f87f93a8403c9c040e9e6e16a035
출처 메모uspto-grants-2012_12