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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1518390Generated: October 26, 2026

4-(4-Methyl-1-piperazinyl)phenol → tert-butyl 6-(8-(benzo[d]thiazol-2-yl((2-(trimethylsilyl)ethoxy)methyl)carbamoyl)-3,4-dihydroisoquinolin-2(1H)-yl)-3-(3-(4-(4-methylpiperazin-1-yl)phenoxy)propyl)picolinate

https://huagongshe.com/reaction/1518390

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Methyl-1-piperazinyl)phenolHCID 11622486—
Reactantethyl 5-(4-((4-(5-amino-1-(tert-butoxycarbonyl)-4-cyano-1H-pyrazol-3-yl)phenoxy)methyl)phenyl)-2-(8-(benzo[d]thiazol-2-yl((2-(trimethylsilyl)ethoxy)methyl)carbamoyl)-3,4-dihydroisoquinolin-2(1H)-yl)thiazole-4-carboxylateHCID 59447596—
Reactanttert-butyl 5-amino-4-cyano-3-(4-hydroxyphenyl)-1H-pyrazole-1-carboxylateHCID 136027725—
ReactantHCID 178450838HCID 178450838—
Producttert-butyl 6-(8-(benzo[d]thiazol-2-yl((2-(trimethylsilyl)ethoxy)methyl)carbamoyl)-3,4-dihydroisoquinolin-2(1H)-yl)-3-(3-(4-(4-methylpiperazin-1-yl)phenoxy)propyl)picolinateHCID 59447636—

Reaction Steps

The title compound 94G was prepared in a similar manner to the synthesis of compound 35A by substituting compound 34D and compound 31F with compound 94F and compound 82A, respectively: ESI (+)LC/MS: 849 (M+H2O—NH4)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232273B2
Source datasetuspto-grants-2012_07
ORD IDord-4081dbce29a242c78e929f79505c22b8
Source noteuspto-grants-2012_07