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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458663Generated: November 1, 2026

Triethylamine → HCID 178470708, compound

https://huagongshe.com/reaction/1458663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl (4-chloro-6-methylpyrimidin-5-yl)acetateHCID 10954591—
ReactantHCID 178445676HCID 178445676—
SolventToluene waterHCID 22272177—
ProductHCID 178470708HCID 178470708—

Reaction Steps

15.2 g (71 mmol) of methyl (4-chloro-6-methylpyrimidin-5-yl)acetate, 11.0 g (71 mmol) of cis-4-tert-butylcyclohexylamine and 20.2 g (0.2 mol) of triethylamine were heated at 80° to 90° C. for 6 hours without solvent. After cooling, the mixture was taken up in water/toluene and the organic phase was dried and concentrated. In the chromatography on silica gel (petroleum ether/ethyl acetate 1:1, then ethyl acetate/methanol 9:1), 5.3 g of chloropyrimidine starting material were first of all retained and then 10.0 g (27.7% of theory) of product were obtained as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05852023
Source datasetuspto-grants-1998_12
ORD IDord-59f59c62c84f402caf8a9d7bef42ea7b
Source noteuspto-grants-1998_12