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HRID 414037Erstellt: 24. Oktober 2026

Hydrochloric Acid → 3-Chloro-N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-2-pyridinesulfonamide-1-oxide

https://huagongshe.com/de/reaction/414037

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktWaterHCID 962—
EduktPhenyl carbamateHCID 69322—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Edukt2-Amino-4,6-dimethoxypyrimidineHCID 118946—
Edukt3-Chloropyridine-2-sulfonamideHCID 14653191—
LösungsmittelAcetonitrileHCID 6342—
Produkt3-Chloro-N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-2-pyridinesulfonamide-1-oxideHCID 14653193—

Reaktionsschritte

To a stirring solution of the N-oxide of 3-chloro-2-pyridinesulfonamide (85 mg, 0.4 mmol) and the phenyl carbamate of 4,6-dimethoxy-2-aminopyrimidine (114 mg, 0.40 mmol) in acetonitrile was added DBU (62 mg, 0.40 mmol). Addition of H2O followed by 5% HCl caused a precipitate to form which was collected, m.p. 144°-147° C. NMR (200 MHz, d6 -DMSO) δ 3.91 (s, 6H), 5.998 (s, 1H), 7.7 (m, 2H), 8.4 (d, 1H), 10.8 (br s, 1H) and 13.1 (br s, 1H); IR (nujol) 1710 (s) cm-1 ; mass spectrum m/e 390 (M+, calc. for C12H12ClN5O6S 389+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04789465
Quelldatensatzuspto-grants-1988_12
ORD IDord-99f0a07897394466824deb4e90cc583d
Quellennotizuspto-grants-1988_12