Triethylamine → HCID 15513658, Verbindung

A suspension of (1-methyl-6-nitro-1H-indol-3-yl)-oxo-acetyl chloride (251 mg, 0.94 mm) and 2-(6-methoxy-1-methyl-1H-indol-3-yl)-acetimidic acid isopropyl ester hydrochloride (280 mg, 0.94 mm) in CH2Cl2(25 mL) was cooled to 0° C., treated with Et3N (0.53 mL, 3.7 mm), and stirred at room temperature while allowing to warm to room temperature overnight. The mixture was then diluted with CH2Cl2 (25 mL), washed with H2O (20 mL), and 0.5 N HCl (20 mL). The combined organic layers were dried over MgSO4, filtered and evaporated. The residue was then combined with toluene (4 mL), cooled to 0° C., treated with pTsOH (197 mg, 1 mm), and stirred for 3 hours. The red solids which precipitated were collected and partitioned between CH2Cl2 (50 mL), and H2O (25 mL). The organic fraction was washed with saturated NaHCO3 solution (25 mL), then dried over MgSO4, filtered and evaporated. Rinsing the residue with tetrahydrofuran (THF) afforded 3-(6-methoxy-1-methyl-1H-indol-3-yl)-4-(1-methyl-6-nitro-1H-indol-3yl)-pyrrole-2,5-dione; mp=308-310° C.; in 31% yield.

1. temperatureto warm to room temperature overnight
2. washwashed with H2O (20 mL), and 0.5 N HCl (20 mL)
3. dry with materialThe combined organic layers were dried over MgSO4
4. filtrationfiltered
5. customevaporated
6. temperaturecooled to 0° C.
7. additiontreated with pTsOH (197 mg, 1 mm)
8. stirringstirred for 3 hours
9. customThe red solids which precipitated
10. customwere collected
11. custompartitioned between CH2Cl2 (50 mL), and H2O (25 mL)
12. washThe organic fraction was washed with saturated NaHCO3 solution (25 mL)
13. dry with materialdried over MgSO4
14. filtrationfiltered
15. customevaporated
16. washRinsing the residue with tetrahydrofuran (THF)

ORD-Eintrag

ord-fbcf18f5c2a94ff8b9a9b18a789c58e6

Quelldatensatz

uspto-grants-2001_05

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US06228877B1