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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 731283생성일: 2026년 10월 24일

Dicyclohexylcarbodiimide → Ethyl cyclopentanecarboxylate

https://huagongshe.com/ko/reaction/731283

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참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물2H-1,2,4-Benzothiadiazine-3-acetic acid, 7-[(methylsulfonyl)amino]-, 1,1-dioxideHCID 24858539—
반응물HCID 57671252HCID 57671252—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물Ethyl cyclopentanecarboxylateHCID 79550—

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온도25 °C

반응 단계

To a solution of cis-2-(3-methylbutylamino)-cyclopentanecarboxylic acid ethyl ester (53.5 mg, 0.237 mmol) in N,N-dimethylformamide (3.0 mL) was added (7-methanesulfonylamino-1,1-dioxo-1,4-dihydro-1λ6-benzo[1,2,4]thiadiazin-3-yl)-acetic acid (prepared as described in Example 1j, 157.4 mg, 0.472 mmol) and a 1.0 M solution of N,N′-dicyclohexylcarbodiimide in dichloromethane (0.47 mL, 0.47 mmol). After stirring at 25° C. for 12 h, the mixture was diluted with dichloromethane and the precipitated N,N′-dicyclohexylurea byproduct was removed by filtration. The filtrate was concentrated and dried in vacuo to afford the crude product, cis-2-[2-(7-methanesulfonylamino-1,1-dioxo-1,4-dihydro-1λ6-benzo[1,2,4]thiadiazin-3-yl)-acetyl]-(3-methylbutyl)amino]-cyclopentanecarboxylic acid ethyl ester, which was used in the next step without further purification. LC-MS (ESI) calcd for C23H34N4O7S2 542.19, found 543.2 [M+H+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07582626B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-f3d843cb606a46d9b5f9a5b3770c9a7c
출처 메모uspto-grants-2009_09