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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692806Generated: October 26, 2026

1-Methyl-4-(methylamino)piperidine → 5-Chloro-N-methyl-N-(1-methylpiperidin-4-yl)-7-morpholinothiazolo[4,5-d]pyrimidin-2-amine

https://huagongshe.com/reaction/1692806

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-4-(methylamino)piperidineHCID 566323—
Reactant5-Chloro-2-(methylsulfonyl)-7-morpholinothiazolo[4,5-d]pyrimidineHCID 57685406—
SolventTriethylamineHCID 8471—
Product5-Chloro-N-methyl-N-(1-methylpiperidin-4-yl)-7-morpholinothiazolo[4,5-d]pyrimidin-2-amineHCID 86630085—

Reaction Steps

Alternatively, 5-chloro-2-(methylsulfonyl)-7-morpholinothiazolo[4,5-d]pyrimidine was reacted with 1-methyl-4-(methylamino)piperidine, without triethylamine, via General Procedure C, to give crude 5-chloro-N-methyl-N-(1-methylpiperidin-4-yl)-7-morpholinothiazolo[4,5-d]pyrimidin-2-amine, which was then reacted with 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine via General Procedure C again to give 144 after purification by silica gel chromatography. MS (Q1) 441 (M+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158626B2
Source datasetuspto-grants-2012_04
ORD IDord-ccc81762d9e2463a869ca8aaffe412b0
Source noteuspto-grants-2012_04