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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 470840생성일: 2026년 10월 26일

Triethylamine → HCID 67006811, 화합물

https://huagongshe.com/reaction/470840

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-BromobenzohydrazideHCID 22219—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물(3-Chloro-4-cyano-2-methylphenyl)-D-threonineHCID 57908671—
용매TetrahydrofuranHCID 8028—
생성물HCID 67006811HCID 6700681176.2%

반응 조건

온도-20 °C

반응 단계

(2R,3S)-2-(3-chloro-4-cyano-2-methylphenylamino)-3-hydroxybutanoic acid (5.0 g, 18.6 mmol), 4-bromobenzhydrazide (CAS 5933-32-4, 4.0 g, 18.6 mmol) and 1-Hydroxybenzotriazole hydrate (2.52 g, 18.6 mmol) were placed in a 250 mL round bottomed flask. Anhydrous THF (120 mL) was added and the mixture was cooled to −20° C. N-(3-Dimethylaminopropyl)-N′-ethylcarbodimide HCl (5.35 g, 27.9 mmol) was added, Followed by Et3N (3.9 mL, 28.0 mmol). The reaction mixture was stirred at −20° C. for 1 h and room temperature for overnight. The reaction was quenched by adding water and extracted with EtOAc, which was washed with 5% aqueous NaOH, water, brine and dried over Na2SO4. The extracts were filtered and the filtrate was concentrated to provide a brown solid, which was purified by flash chromatography washed with 80% EtOAc in hexanes to afford the title compound (6.6 g, 76%). 1H NMR (400 MHz, acetone-d6, δ in ppm) 7.87 (d, J=8.6 Hz, 2H), 7.71 (d, J=8.6 Hz, 2H), 7.54 (d, J=8.6 Hz, 1H), 6.67 (d, J=8.6 Hz, 1H), 5.55 (d, J=7.4 Hz, 1H), 4.39 (m, 1H), 4.10 (dd, J=3.3, 7.4 Hz, 1H), 2.36 (s, 3H), 1.35 (d, J=6.4 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08629167B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-ca5560ab2d324a59a4d6fdad2ecc5df8
출처 메모uspto-grants-2014_01