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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 486755생성일: 2026년 10월 24일

Diisopropylethylamine → HCID 22850667, 화합물

https://huagongshe.com/ko/reaction/486755

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Dipentylcarbamyl chlorideHCID 22106956—
반응물(S)-1-[N-(3-Chlorophenyl)-N-phenylcarbamoyl]-piperazine-2-carboxylic acid hydrobromideHCID 70072107—
용매DichloromethaneHCID 6344—
생성물HCID 22850667HCID 2285066737.1%

반응 조건

온도25 °C

반응 단계

To a suspension of 1.05 g (2.3 mmole) of (S)-1-[N-(3-chlorophenyl)-N-phenylcarbamoyl]piperazine-2-carboxylic acid hydrobromide (from Step C) in 20 ml of methylene chloride was added 1.23 g (9.5 mmole) of N,N-diisopropylethylamine followed by the dropwise addition of a solution of 523 mg (2.38 mmole) of dipentylcarbamoyl chloride (from Example 3, Step A) in 5 ml of methylene chloride. After stirring 24 hours at 25° C., the solution was extracted with 2N HCl, then H2O and dried over MgSO4. The dried methylene chloride solution was concentrated in vacuo and the residue was dissolved in isopropyl ether and was diluted with Petroleum ether bp. 30°-60° C.) until cloudy. The oil which precipitated was then decanted, redissolved in isopropanol and concentrated in vacuo to yield 464 mg (36%) of (S)-1-[N-(3-chlorophenyl)-N-phenylcarbamoyl]-4-(dipentylcarbamoyl)piperazine-2-carboxylic acid as a glassy solid; TLC showed a single spot, Rf 0.75 (Anal tech SGF plates developed with isoamyl alcohol:acetone:water [5:2:1]).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05292726
출처 데이터셋uspto-grants-1994_03
ORD IDord-4d8ef0719f034fc58c6de681e1b5c720
출처 메모uspto-grants-1994_03