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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206847Generated: November 1, 2026

5-Chloro-2-methanesulfonylpyrimidine-4-carboxylic acid → HCID 89825775, compound

https://huagongshe.com/reaction/2206847

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2-methanesulfonylpyrimidine-4-carboxylic acidHCID 1241459—
Reactant1-Aminotetralin, (R)-HCID 7058072—
Reactantalpha-CyclohexylcyclohexanemethanamineHCID 10774245—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 89825775HCID 8982577531%

Reaction Steps

0.20 g (0.84 mmol) of 5-chloro-2-(methylsulfonyl)pyrimidine-4-carboxylic acid, 0.15 g (1.01 mmol) of (1R)-1,2,3,4-tetrahydronaphthalene-1-amine and 0.33 g (1.69 mmol) of dicyclohexylmethylamine in 1.5 ml of N-methylpyrrolidone are heated in a closed cuvette in the microwave at 150° C. for 30 minutes (Biotage Initiator, http://www.biotage.com/DynPage.aspx?id=22001). The crude mixture obtained in this manner is applied to silica gel and purified by column chromatography using the mobile phase heptane/ethyl acetate. Concentration gives initially 0.024 g of 5-chloro-N-[(1R)-1,2,3,4-tetrahydronaphthalen-1-yl]pyrimidine-2-amine (solid) and then 0.08 g of 2-(methylsulfonyl)-N-[(1R)-1,2,3,4-tetrahydronaphthalen-1-yl]pyrimidine-5-amine (wax-like, yield 31% at a purity of 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09375002B2
Source datasetuspto-grants-2016_06
ORD IDord-aefd7fc2867a47aa9066c4d64f853a9b
Source noteuspto-grants-2016_06