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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036165Generated: November 2, 2026

Diisopropylethylamine → 7-[(R)-2-(naphthalen-1-yloxymethyl)pyrrolidin-1-yl]-[1,2,4]-triazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/1036165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant7-Chloro[1,2,4]triazolo[1,5-a]pyrimidineHCID 21766612—
Reactant(R)-2-(naphthalen-1-yloxymethyl)pyrrolidineHCID 46845432—
Solvent1-ButanolHCID 263—
Product7-[(R)-2-(naphthalen-1-yloxymethyl)pyrrolidin-1-yl]-[1,2,4]-triazolo[1,5-a]pyrimidineHCID 46842838—

Reaction Steps

400 mg of (R)-2-(naphthalen-1-yloxymethyl)pyrrolidine, 500 mg of the 7-chloro-[1,2,4]triazolo[1,5-a]pyrimidine prepared above and 650 mg of N-ethyldiisopropylamine are heated at 130° C. in a microwave for 3 h in 40 ml of 1-butanol. The butanol is subsequently removed in vacuo, the residue is taken up in ethyl acetate, mixed with water, adjusted to pH 12 using 1 N NaOH solution, phases are separated, the organic phase is dried over sodium sulfate, evaporated and chromatographed on silica gel, giving 640 mg of “A1”; m.p. 74-75°;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546406B2
Source datasetuspto-grants-2013_10
ORD IDord-8a5b501d001b44a7a4ad7671b0cd41dd
Source noteuspto-grants-2013_10