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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470731Generated: November 1, 2026

Diisopropylethylamine → (S)-2-{4-[4-(1-Acetylamino-ethyl)-phenyl]-piperidin-1-yl}-pyrimidine-5-carboxylic acid

https://huagongshe.com/reaction/1470731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 2-chloropyrimidine-5-carboxylateHCID 12627752—
Reactant(S)-N-[1-(4-piperidin-4-yl-phenyl)ethyl]-acetamideHCID 67125412—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product(S)-2-{4-[4-(1-Acetylamino-ethyl)-phenyl]-piperidin-1-yl}-pyrimidine-5-carboxylic acidHCID 67125410—

Reaction Conditions

Temperature100 °C

Reaction Steps

To 1.52 g (8.5 mmol) 2-chloropyrimidine-5-carboxylic acid methyl ester in 80 mL NMP are added 2.1 g (8.5 mmol (S)—N-[1-(4-piperidin-4-yl-phenyl)-ethyl]-acetamide (V.1) and 2.9 mL (17.1 mmol) DIPEA and the mixture is stirred for 4 h at 100° C. The solvent is removed in vacuo. The residue is treated with 100 mL MeOH and 10 mL 4N sodium hydroxide solution is added. The mixture is stirred for 1 h at 60° C. After cooling to rt 4N HCl solution is added until the pH is acidic. The precipitate is collected and dried to yield the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006450B2
Source datasetuspto-grants-2015_04
ORD IDord-0016a09d847c4769af0ad2bf9bc1ac8c
Source noteuspto-grants-2015_04