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HRID 326346Erstellt: 24. Oktober 2026

Hydrochloric Acid → Isopropyl 2-chloro-5-[(6-methyl-2,3-dihydro-1,4-dithiine-5-carbonyl)amino]benzoate

https://huagongshe.com/de/reaction/326346

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktThionyl ChlorideHCID 24386—
EduktIsopropyl 5-amino-2-chlorobenzoateHCID 369590—
Edukt2-Carboxy-3-methyl-5,6-dihydro-1,4-dithiinHCID 600502—
LösungsmittelPyridineHCID 1049—
LösungsmittelTolueneHCID 1140—
LösungsmittelDichloromethaneHCID 6344—
ProduktIsopropyl 2-chloro-5-[(6-methyl-2,3-dihydro-1,4-dithiine-5-carbonyl)amino]benzoateHCID 50328157%

Reaktionsschritte

Thionyl chloride (6.5 g, 0.055 mole) was added slowly to a stirred solution of 5,6-dihydro-3-methyl-1, 4-dithiin-2-carboxylic acid (3 g, 0.017 mole) in toluene (15 ml) at room temperature. The mixture was heated under reflux for 4 hours. The excess toluene and thionyl chloride were removed in a rotary evaporator, yielding the crude acid chloride. 1-Methylethyl 5-amino-2-chlorobenzoate (3 g, 0.014 mole) in pyridine (20 ml) was added slowly to a stirred solution of the crude acid chloride (3 g) in methylene chloride (20 ml) at 20° C. The mixture was stirred for 24 hours, poured onto ice and concentrated hydrochloric acid, washed twice with water, dried with magnesium sulfate, and the methylene chloride evaporated. Recrystallization from 95% ethanol yielded the title compound, m.p. 122°-124° C. (3 g, 57% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05268389
Quelldatensatzuspto-grants-1993_12
ORD IDord-1ba1a775bcdf4435b640ee5cafae3508
Quellennotizuspto-grants-1993_12