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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 4135Erstellt: 23. Oktober 2026

2-Amino-4-methoxy-6-methyl-1,3,5-triazine → 2-(Dichloromethyl)-N-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]benzenesulfonamide

https://huagongshe.com/de/reaction/4135

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Amino-4-methoxy-6-methyl-1,3,5-triazineHCID 15466—
Edukt2-(Dichloromethyl)benzenesulfonyl isocyanateHCID 20152700—
LösungsmittelAcetonitrileHCID 6342—
Produkt2-(Dichloromethyl)-N-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]benzenesulfonamideHCID 13364623—

Reaktionsschritte

2-(Dichloromethyl)benzenesulfonyl isocyanate prepared from 10 mmol of sulfonamide as described in the synthesis of Example 1, was treated with acetonitrile (15 ml) and 2-amino-4-methoxy-6-methyl-1,3,5-triazine (1.40 g). The mixture was stirred for 18 hrs. and filtered. The filtrate was evaporated and recrystallized from acetone to give 0.78 g of white solid, mp 168°-169° (dec). 1H nmr δDMSO-d6TMS 8.37-7.50 (m, featuring singlet at 8.07), 7.00-6.17 (brds), 4.00 (s), 2.48 (s). IR (nujol) featured bands at 1720 and 1590 cm-1. Mass spectrum featured 264.9367 (calc'd for C8H5Cl2NO3S 264.9367) and 140.0687 (calc'd for C5H8N4O 140.0697).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04723990
Quelldatensatzuspto-grants-1988_02
ORD IDord-a13c037be7c241d6a705a7e8083f6b1a
Quellennotizuspto-grants-1988_02