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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421583Generated: October 27, 2026

Diisopropylethylamine → HCID 178526829, compound

https://huagongshe.com/reaction/421583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-chloro-N-cyclopentyl-5-nitropyrimidin-4-amineHCID 7147253—
ReactantHCID 178511715HCID 178511715—
SolventDimethylformamideHCID 6228—
ProductHCID 178526829HCID 17852682988.1%

Reaction Steps

(2-Chloro-5-nitropyrimidin-4-yl)cyclopentylamine (6.18 mmol, 1.5 g.) and trans-4-aminocyclohexan-1-ol (7.42 mmol, 854 mg mL) were mixed in DMF (18 mL) and N,N-diisopropylethylamine (7.42 mmol, 1.29 mL) was added. The reaction mixture was stirred overnight. Solvent was removed in vacuo and the residue purified using column chromatography (SiO2, 1:1 n-hexanes/ethyl acetate→7:3 n-hexanes/ethyl acetate→ethyl acetate) to give the desired product (1.75 g, 88% yield). ES-MS: 322 (M+1). When the hydrochloride salt of an amine is used in place of the trans-4-aminocyclohexan-1-ol described above, 2 to 3 equivalents of N,N-diisopropylethylamine or sodium bicarbonate and tetrahydrofuran or acetonitrile were used as solvent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101588B2
Source datasetuspto-grants-2012_01
ORD IDord-3da1827b2fbf4ac8b0f1adc16fe2be4b
Source noteuspto-grants-2012_01