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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772647Generated: November 2, 2026

Tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine-1-carboxylate → tert-Butyl 4-(2-(hydroxymethyl)-8-morpholinoimidazo[1,2-a]pyrazin-5-yl)-5,6-dihydropyridine-1(2H)-carboxylate

https://huagongshe.com/reaction/1772647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine-1-carboxylateHCID 4642098—
Reactant(5-Bromo-8-morpholinoimidazo[1,2-a]pyrazin-2-yl)methanolHCID 117727888—
Producttert-Butyl 4-(2-(hydroxymethyl)-8-morpholinoimidazo[1,2-a]pyrazin-5-yl)-5,6-dihydropyridine-1(2H)-carboxylateHCID 117733768—

Reaction Steps

Compound 1e was subjected to Suzuki coupling reaction conditions with N-Boc-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester using the method described in Example 1, Step G to obtain compound 26a. Mass Spectrum (LCMS, ESI pos.) Calcd. for C21H29N5O4: 416.2 (M+H). Found 416.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249163B2
Source datasetuspto-grants-2016_02
ORD IDord-13f616338bc24f578a0397b79d07fef6
Source noteuspto-grants-2016_02