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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11582생성일: 2026년 10월 25일

Hydrochloric Acid → (s)-1-(2-Hydroxyethyl)-3-(5-chloroindole-2-carbonylamino)-3,4-dihydrocarbostyril

https://huagongshe.com/reaction/11582

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Ethyl AcetateHCID 8857—
반응물(S)-1-carboxymethyl-3-(5-chloroindole-2-carbonylamino)-3,4-dihydrocarbostyrilHCID 69195122—
용매BoraneHCID 6331—
용매TetrahydrofuranHCID 8028—
생성물(s)-1-(2-Hydroxyethyl)-3-(5-chloroindole-2-carbonylamino)-3,4-dihydrocarbostyrilHCID 6919491819%

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온도35 °C

반응 단계

A mixture of (S)-1-carboxymethyl-3-(5-chloroindole-2-carbonylamino)-3,4-dihydrocarbostyril (Example 10) (6 mg) in 1.0 M borane in tetrahydrofuran solution (2 mL) under argon was stirred at 35° C. for 3 h. After cooling to room temperature, 1.0 M aqueous hydrochloric acid (10 mL) and ethyl acetate (10 mL) were added. This mixture was stirred for 3 h before the layers were separated. The organic phase was washed with water (10 mL three times) and evaporated under vacuum. The residue was chromatographed on reverse phase preparative HPLC to isolate the title compound (1.1 mg) and the over-reduction product (S)-1-(2-hydroxyethyl)-3-(5-chloroindole-2-carbonylamino)-1,2,3,4-tetrahydroquinoline (0.9 mg). Title compound HPLC/MS [M+H]+, 384.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098235B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-53c7f65f8f8a484284f4f588533f0f5f
출처 메모uspto-grants-2006_08