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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 480326생성일: 2026년 10월 24일

Diisopropylethylamine → (3-{[(Benzo[1,2,5]oxadiazole4-sulfonyl)-(4-butyl-benzyl)-amino]-methyl}-phenyl)-acetic acid methyl ester

https://huagongshe.com/ko/reaction/480326

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물2,1,3-Benzoxadiazole-4-sulfonyl chlorideHCID 2735446—
반응물(3-((4-Butyl-benzylamino)-methyl)-phenyl)-acetic acid methyl esterHCID 54268705—
용매1,2-DichloroethaneHCID 11—
용매Ethyl AcetateHCID 8857—
생성물(3-{[(Benzo[1,2,5]oxadiazole4-sulfonyl)-(4-butyl-benzyl)-amino]-methyl}-phenyl)-acetic acid methyl esterHCID 69544491—

반응 단계

Benzofurazan4-sulfonyl chloride (109 mg, 0.50 mmol) was added to a solution of {3-[(4-butyl-benzylamino)-methyl]-phenyl}-acetic acid methyl ester (163 mg, 0.50 mmol) and N,N-diisopropylethylamine (65 mg, 0.50 mmol) in 1,2-dichloroethane. The reaction mixture was stirred at room temperature for 20 h. The reaction was diluted with EtOAc and the organic solution was washed with water followed by brine. The organic solution was dried over MgSO4, filtered, and concentrated to afford (3-{[(benzo[1,2,5]oxadiazole4-sulfonyl)-(4-butyl-benzyl)-amino]-methyl}-phenyl)-acetic acid methyl ester. 1H NMR (400 MHz, CDCl3) δ 7.95 (d, 1H), 7.88 (d, 1H), 7.37-7.41 (m, 1H), 7.06-7.10 (m, 2H), 6.90-6.97 (m, 6H), 4.56 (s, 2H), 4.51 (s, 2H), 3.66 (s, 3H), 3.45 (s, 2H), 2.48 (t, 2H), 1.45-1.53 (m, 2H), 1.23-1.32 (m, 2H), 0.89 (t, 3H); MS 508 (M+18).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06649657B2
출처 데이터셋uspto-grants-2003_11
ORD IDord-cc5cfc699f664406b2956d019ede86e7
출처 메모uspto-grants-2003_11