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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200899Generated: October 30, 2026

Ethyl 4-((3-chloro-4-methoxybenzyl)amino)-2-(methylsulfanyl)pyrimidine-5-carboxylate → HCID 117622625, compound

https://huagongshe.com/reaction/2200899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-((3-chloro-4-methoxybenzyl)amino)-2-(methylsulfanyl)pyrimidine-5-carboxylateHCID 22025927—
ReactantHCID 117622626HCID 117622626—
ProductHCID 117622625HCID 11762262554%

Reaction Steps

The procedures were analogous to Example 1(2). Ethyl 4-((3-chloro-4-methoxybenzyl)amino)-2-(5-azaspiro[2.4]heptan-5-yl)pyrimidine-5-carboxylate (3.4 g, 8.17 mmol) was used in step 2 instead of ethyl 4-((3-chloro-4-methoxybenzyl)amino)-2-(methylthio)pyrimidine-5-carboxylate. Yield: 54%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359371B2
Source datasetuspto-grants-2016_06
ORD IDord-d8905dcccd924b2293092206cd0909ec
Source noteuspto-grants-2016_06