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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1181722생성일: 2026년 10월 27일

Diethyl cyanophosphonate → 5-{2-[(5-chloro-1H-indol-3-yl)methyl]-7-isobutyl-5-methyl-4,6-dioxo-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-d]pyrimidin-3-yl}-1-methyl-N-(pyridin-4-ylmethyl)-1H-pyrrole-3-carboxamide

https://huagongshe.com/reaction/1181722

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl cyanophosphonateHCID 76257—
반응물4-(Methylamino)pyridineHCID 123098—
반응물5-{2-[(5-chloro-1H-indol-3-yl)methyl]-7-isobutyl-5-methyl-4,6-dioxo-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-d]pyrimidin-3-yl}-1-methyl-1H-pyrrole-3-carboxylic acidHCID 58981063—
생성물5-{2-[(5-chloro-1H-indol-3-yl)methyl]-7-isobutyl-5-methyl-4,6-dioxo-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-d]pyrimidin-3-yl}-1-methyl-N-(pyridin-4-ylmethyl)-1H-pyrrole-3-carboxamideHCID 58981047—

반응 단계

This compound was synthesized by the reaction of 5-{2-[(5-chloro-1H-indol-3-yl)methyl]-7-isobutyl-5-methyl-4,6-dioxo-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-d]pyrimidin-3-yl}-1-methyl-1H-pyrrole-3-carboxylic acid and pyridin-4-yl-methylamine using diethyl cyanophosphonate as a coupling reagent. Mass: 599.15 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07285558B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-15a29db017b643588d370abb3997a45c
출처 메모uspto-grants-2007_10