Reaktion #88558

Reaktionsgleichung

hydrochloric acid

HBr

(S)-tert-butyl 1-(3-fluoro-6-cyano-9-((2-(trimethylsilyl)ethoxy)methyl)-9H-dipyrido[2,3-b;4′,3′-d]pyrrol-4-yl)pyrrolidin-3-yl(ethyl)carbamate

sodium hydroxide

→

title compound

Ausbeute 77.1%

(S)-3-Fluoro-4-(3-(ethylamino)pyrrolidin-1-yl)-9H-dipyrido[2,3-b;4′,3′-d]pyrrole-6-carbonitrile

Ausbeute 77.1%

Lösungsmittel

1,4-dioxane

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe cooled reaction mixture
2. 2
   Sonstigeproducing a cloudy precipitate
3. 3
   SonstigeThe solid was collected by centrifugation
4. 4
   workup.DISSOLUTIONdissolved in dimethylsulfoxide (2 mL)
5. 5
   Sonstigepurified by preparative HPLC [5-85% methanol in water (0.1% ammonium hydroxide) over 30 min, 35 mL/min]

Vorschrift

(S)-tert-butyl 1-(3-fluoro-6-cyano-9-((2-(trimethylsilyl)ethoxy)methyl)-9H-dipyrido[2,3-b;4′,3′-d]pyrrol-4-yl)pyrrolidin-3-yl(ethyl)carbamate (120 mg, 0.2 mmol) was dissolved in 1,4-dioxane (0.3 mL) and then treated with 48% HBr(aq) (0.3 mL) and heated at 55° C. for 20 minutes. The cooled reaction mixture was then basified to pH ˜12 by dropwise addition of 6N sodium hydroxide and then immediately acidified to pH ˜8-9 by dropwise addition of concentrated hydrochloric acid, producing a cloudy precipitate. The solid was collected by centrifugation, dissolved in dimethylsulfoxide (2 mL), and purified by preparative HPLC [5-85% methanol in water (0.1% ammonium hydroxide) over 30 min, 35 mL/min] to afford the title compound as a pale yellow solid (50 mg, 30% over two steps). 1H NMR (500 MHz, d6-DMSO) δ 8.87 (s, 1H), 8.49 (s, 1H), 8.32 (d, J=7.0, 1H), 3.91-3.84 (m, 1H), 3.83-3.76 (m, 2H), 3.58 (m, 1H), 3.43 (m, 1H), 2.67-2.56 (m, 2H), 2.19 (m, 1H), 1.83 (m, 1H), 1.07 (t, J=7.1, 3H), NH signal not observed. LCMS (Method D): RT=6.033 min, M+H+=325.1.

Quelle