Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 709438Erstellt: 27. Oktober 2026

Proton sponge → (S)-3-isopropyl-6-((1-(o-tolyl)ethyl)amino)pyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/reaction/709438

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktProton spongeHCID 88675—
Edukt(alphaS)-alpha,2-DimethylbenzenemethanamineHCID 197800—
Edukt6-Chloro-3-(propan-2-yl)-1,2,3,4-tetrahydropyrimidine-2,4-dioneHCID 820107—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt(S)-3-isopropyl-6-((1-(o-tolyl)ethyl)amino)pyrimidine-2,4(1H,3H)-dioneHCID 1177641028,1%

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

To a stirred solution of (1S)-1-(2-methylphenyl)ethan-1-amine (310 mg, 2.29 mmol, 1.50 equiv) in NMP (1 mL) was added proton sponge (491.4 mg, 2.30 mmol, 1.50 equiv) and 1.3 (288 mg, 1.53 mmol, 1.00 equiv). The resulting solution was stirred for 1 h at 130° C. in an oil bath, cooled to room temperature, and then diluted with DMSO (2 mL). The solids were filtered and the filtrate was purified by Flash-Prep-HPLC with the following conditions: Column: X Bridge C18, 19*150 mm, 5 um; Mobile Phase A: H2O/0.05% TFA, Mobile Phase B: CH3CN; Flow rate: 20 mL/min; Gradient: 30% B to 70% B in 10 min. This afforded 50 mg of crude product which was subsequently separated by chiral preparative HPLC with the following conditions: Column, Chiralpak IC, 2*25 cm, Sum; mobile phase, hexanes and ethanol (9:1, 15 min). This resulted in 35.6 mg (8%) of the title compound as a white solid. LC/MS: m/z (ES+) 288 (M+H)+. 1H-NMR (300 MHz, DMSO-d6): δ ppm 9.76 (br s, 1H), 7.28 (d, J=7.2 Hz, 1H) 7.24-7.14 (m, 3H), 6.48 (d, J=6.3 Hz, 1H), 4.95-4.86 (m, 1H), 4.60 (quin, J=6.9 Hz, 1H), 4.19 (s, 1H), 2.34 (s, 3H), 1.37 (d, J=6.6 Hz, 3H), 1.27 (d, J=6.9 Hz, 6H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09181200B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-8daa09b225c0443fb61c802a6d203ab6
Quellennotizuspto-grants-2015_11