Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 890786생성일: 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/890786
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 2,1,3-Benzoxadiazole-4-sulfonyl chloride | HCID 2735446 | — |
| 반응물 | (3-((4-Butyl-benzylamino)-methyl)-phenyl)-acetic acid methyl ester | HCID 54268705 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | (3-{[(Benzo[1,2,5]oxadiazole4-sulfonyl)-(4-butyl-benzyl)-amino]-methyl}-phenyl)-acetic acid methyl ester | HCID 69544491 | — |
반응 단계
Benzofurazan-4-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]oxadiazole-4-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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06998423B2 |
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| 출처 데이터셋 | uspto-grants-2006_02 |
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| ORD ID | ord-b18d816721d64d0da63f528d21467f60 |
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| 출처 메모 | uspto-grants-2006_02 |
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