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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1376643생성일: 2026년 10월 24일

Methanesulfonic acid, aminoimino- → HCID 178512793, 화합물

https://huagongshe.com/ko/reaction/1376643

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonic acid, aminoimino-HCID 9877361—
반응물2-(2-carboxyethyl)-8-(5-aminopentynyl)-2,3,4,5-tetrahydro-1H-2-benzazepin-1-one trifluoracetateHCID 22905359—
용매Acetic AcidHCID 176—
생성물HCID 178512793HCID 17851279315.2%

반응 단계

A solution of 2-(2-carboxyethyl)-8-(5-aminopentynyl)-2,3,4,5-tetrahydro-1H-2-benzazepin-1-one trifluoracetate (20 mg, 0.063 mmol) in saturated aqueous KHCO3 (1 mL) was treated with formamidine sulfonic acid (80 mg, 1.0 mmol), and the resulting mixture stirred for 2 hours. The mixture was then treated with acetic acid, and the volatiles were removed. The residue was purified by HPLC (1/2' C-18 reverse-phase column) eluting with a gradient of 3:7 methanol (0.1% trifluoroaceate)/water (0.1% trifluoroaceate), time 0 to 10 min, to 7:3 methanol(0.1% trifluoroaceate)/water(0.1% trifluoroaceate), time 10 to 40 min, to yield 4.5 mg (15%) of 2-(2-carboxyethyl)-8-(5-guanidinopentynyl)-2,3,4,5-tetrahydro-1H-2-benzazepin-1-one trifluoracetate as a light brown solid; 1H NMR(D2O) d7.40(s, 1H), 7.25(dd, J=3, 6 Hz, 1H), 7.15(d, J=6 Hz, 1H), 3.80(t, J=6 Hz, 2H), 3.30(m, 4H), 3.15(t, J=6 Hz, 2H), 2.00(t, J=6 Hz, 2H), 1.80(m, 2H); MS(FAB) m/z=357.1(MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05663166
출처 데이터셋uspto-grants-1997_09
ORD IDord-fcfd52be8c89493b9fd79073eb494998
출처 메모uspto-grants-1997_09