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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1884018생성일: 2026년 10월 26일

Hydrochloric Acid → N-(4-(((3-amino-1,2-dihydro-1-oxobenzo[f]quinazolin-9-yl)-amino)sulfonyl)benzoyl)-L-glutamic acid

https://huagongshe.com/reaction/1884018

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물diethyl N-(4-(((3-amino-1,2-dihydro-1-oxobenzo[f]quinazolin-9-yl)amino)sulfonyl)benzoyl)-L-glutamateHCID 136147908—
용매Sodium HydroxideHCID 14798—
생성물N-(4-(((3-amino-1,2-dihydro-1-oxobenzo[f]quinazolin-9-yl)-amino)sulfonyl)benzoyl)-L-glutamic acidHCID 136076379—

반응 조건

온도50 °C

반응 단계

A solution of diethyl N-(4-(((3-amino-1,2-dihydro-1-oxobenzo[f]quinazolin-9-yl)amino)sulfonyl)benzoyl)-L-glutamate (0.175 g, 0.3 mmoles) in 1 N NaOH (12 ml) was stirred and heated to 50° C. under a nitrogen atmosphere for 24 hrs. After cooling,the solution was acidified (pH 3) with concentrated HCl to cause precipitation of the product which was filtered, washed with water and dried to give N-(4-(((3-amino-1,2-dihydro-1-oxobenzo[f]quinazolin-9-yl)-amino)sulfonyl)benzoyl)-L-glutamic acid as an off-white solid. (0.18 g, 99%) 1H NMR (DMSO-d6, 300 MHz) δ: 1.81-2.13 (m, 2H, glu-CH2); 2.32 (t, J=7.6 Hz, 2H, glu-CH2); 4.34 (m, 1H, glu-CH); 6.58 (br s, 2H, NH2); 7.16 (d, J=8.9 Hz, 1H, Ar); 7.22 (dd, J=8.6, 2 Hz, 1H, Ar); 7.74 (d, J=8.7 Hz, 1H, Ar); 7.89 (d, J=9.0 Hz, 1H, Ar); 7.96 (m, 4H, Ar); 8.78 (d, J=7.6 Hz, 1H, glu-NH); 9.49 (d, J=2 Hz, 1H, Ar); 10.68 (s, 1H, NH); 11.1 (br s, 1H, NH); 12.3 (br s, 2H, (CO2H)2). Anal. Calculated for C24H21N5O8S.3H2O: C, 48.56; H, 4.58; N, 11.80; S, 5.40. Found: C, 48.38; H, 4.30; N, 11.69; S. 5.34.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06762188B1
출처 데이터셋uspto-grants-2004_07
ORD IDord-1c5b39da56a24ea4a3ed78338c0ab301
출처 메모uspto-grants-2004_07