Hydrochloric Acid → 1-(4,5-dihydro-1H-imidazol-2-ylmethyl)-3-methanesulfonyl-6-methyl-1H-indole

HRID 23381

Reaktionsgleichung

[CH3:1][S:2]([C:5]1[C:13]2[C:8](=[CH:9][C:10]([CH3:14])=[CH:11][CH:12]=2)[N:7]([CH2:15][C:16]#[N:17])[CH:6]=1)(=[O:4])=[O:3].CC1C=C2C([CH:23]=[CH:24][NH:25]2)=CC=1.C(N)CN.Cl>CO.C(O)C.O.C(=S)=S>[NH:17]1[CH2:23][CH2:24][N:25]=[C:16]1[CH2:15][N:7]1[C:8]2[C:13](=[CH:12][CH:11]=[C:10]([CH3:14])[CH:9]=2)[C:5]([S:2]([CH3:1])(=[O:4])=[O:3])=[CH:6]1

Komponenten

Reaktionsbedingungen

Temperatur: 142 °C

Versuchsvorschrift

(3-Methanesulfonyl-6-methyl-indol-1-yl)-acetonitrile (0.4 g, 1.611 mmole) prepared from 6-methylindole as described in Steps 1-4 above, was added to ethylene diamine (4.3 ml, 438 mmole) in a reaction tube. A single drop of carbon disulfide was carefully added. The mixture was heated in a microwave reactor at 142° C. for 30 minutes. Upon cooling, the reaction mixture was poured into a mixture of ice and water, stirred 20 minutes and filtered. The colorless precipitate collected was washed with water (20 ml) and dried under vacuum at room temperature. The free base thus obtained (420 mg, 90% yield) was converted into the hydrochloride salt by first dissolving in methanol and then adding an excess of HCl in ethanol. The mixture was stripped to dryness and recrystallized from a mixture of ethyl acetate-methanol to afford 344 mg of 1-(4,5-dihydro-1H-imidazol-2-ylmethyl)-3-methanesulfonyl-6-methyl-1H-indole, mp >300° C. as the hydrochloride salt.

Aufarbeitung

temperatureUpon cooling
filtrationfiltered
customThe colorless precipitate collected
washwas washed with water (20 ml)
customdried under vacuum at room temperature
customThe free base thus obtained (420 mg, 90% yield)
customrecrystallized from a mixture of ethyl acetate-methanol

Quellen und Nachweise

ORD-Eintrag: ord-f263b8a22ad24836ac45316e00c6321c
Quelldatensatz: uspto-grants-2005_02
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US06852726B2

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