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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17191생성일: 2026년 10월 24일

Sodium Thiosulfate → Tert-butyl 4-(4-amino-7-iodofuro[3,2-c]pyridin-3-yl)-2-methoxyphenylcarbamate

https://huagongshe.com/ko/reaction/17191

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ThiosulfateHCID 24477—
반응물N-IodosuccinimideHCID 120273—
반응물Tert-butyl 4-(4-aminofuro[3,2-c]pyridin-3-yl)-2-methoxyphenylcarbamateHCID 18451465—
용매DimethylformamideHCID 6228—
생성물Tert-butyl 4-(4-amino-7-iodofuro[3,2-c]pyridin-3-yl)-2-methoxyphenylcarbamateHCID 1845146084%

반응 단계

N-Iodosuccinimide (0.333 g, 1.48 mmol) was added to a solution of tert-butyl 4-(4-aminofuro[3,2-c]pyridin-3-yl)-2-methoxyphenylcarbamate (0.439 g, 1.24 mmol) in N,N-dimethylformamide (10 mL) at ambient temperature. The reaction suspension was stirred for 18 hours, at which time no starting material remained. An aqueous solution of 10% sodium thiosulfate (10 mL) was added to the suspension and stirred for 30 minutes. The precipitate was collected by vacuum filtration and washed with water. The solid was dried in vacuo to give the title compound (0.501 g, 84%) as a tan solid. 1H NMR (DMSO-d6, 400 MHz) δ 8.08 (s, 1H), 8.07 (s, 1H), 8.06 (s, 1H), 7.85 (d, 1H), 7.13 (d, 1H), 7.04, (dd, 1H), 5.73-5.80 (bs, 2H), 3.86 (s, 3H), 1.48 (s, 9H); RP-HPLC (Conditions d) Rt 8.49 min.; MS: MH+ 482.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737160B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-c8c124ac2a8e4858b3b50ed0ef9d7251
출처 메모uspto-grants-2010_06