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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1949879생성일: 2026년 10월 25일

Oxalyl chloride → 4,5-Dihydro-6-oxa-1-thia-3-aza-benzo[e]azulene-2-carboxylic acid (2-chloro-phenyl)-methyl-amide

https://huagongshe.com/reaction/1949879

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물Benzenamine, 2-chloro-N-methyl-HCID 136736—
반응물4,5-Dihydro-6-oxa-1-thia-3-aza-benzo[e]azulene-2-carboxylic acidHCID 86634848—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물4,5-Dihydro-6-oxa-1-thia-3-aza-benzo[e]azulene-2-carboxylic acid (2-chloro-phenyl)-methyl-amideHCID 5790049430%

반응 단계

To a suspension of 4,5-dihydro-6-oxa-1-thia-3-aza-benzo[e]azulene-2-carboxylic acid (1 eq, 0.38 mmol, 101 mg) in anhydrous DCM (3 ml), 1 drop of DMF was added, followed by 2M oxalyl chloride in DCM (1.7 eq, 0.65 mmol, 330 ul) dropwise. Effervescence was seen and the reaction was stirred at room temperature for 40 mins before evaporating in vacuo. The crude material was dissolved in DCM (3 ml) and 2-chloro-N-methyl aniline (2 eq, 0.76 mmol, 94 ul) was added. The reaction was stirred at room temperature for 16 hr and extracted into DCM, washed with aq K2CO3, the organic layer dried over MgSO4, filtered, and purified on silica (ISCO, gradient 0% ethyl acetate/petrol to 25% ethyl acetate/petrol) to give 326 as a white solid (42 mg, yield 30%). 1H NMR DMSO, 2.89-2.92 (2H, m), 3.43 (3H, s), 4.23 (2H, br. m), 7.02 (1H, d, J=8.4), 7.08 (1H, t, J=7.6), 7.26 (1H, t, J=8), 7.38-7.41 (2H, m), 7.48-7.51 (2H, m), 7.58 (1H, d, J=8.4). MS: (ESI+): MH+ 371, purity >95%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08399690B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-7b098a56c17949d49a1e5b2707050a55
출처 메모uspto-grants-2013_03