Реакция #69301

Уравнение реакции

triethylamine

(1RS,3SR)-1-(3-hydroxy-phenyl)-6-(2-methoxy-ethoxy)-3-methyl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester

2-dimethylaminoethyl amine

sodium carbonate

→

(3aSR,10RS)-2-(2-Dimethylamino-ethyl)-10-(3-hydroxy-phenyl)-6-(2-methoxy-ethoxy)-3a-methyl-3a,4,9,10-tetrahydro-2,9,10a-triaza-cyclopenta[b]fluorene-1,3-dione

Растворители

dichloromethane

dichloromethane

dichloromethane

Water

Условия реакции

Обработка

1. 1
   ТемператураThe solution is cooled again to 0° C.
2. 2
   Температураto warm up to room temperature over night
3. 3
   Экстракцияthe aqueous layer is extracted with dichloromethane
4. 4
   СушкаThe combined organic layers are dried with magnesium sulphate
5. 5
   Другоеthe solvent is removed under reduced pressure (210 mg crude intermediate)

Методика

To a suspension of 100 mg (240 μmol) (1RS,3SR)-1-(3-hydroxy-phenyl)-6-(2-methoxy-ethoxy)-3-methyl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester in 4 ml dichloromethane are added 126 μl (970 μmol, 4.00 eq.) triethylamine. The solution is cooled to 0° C. and a solution of 123 mg (610 μmol, 2.5 eq.) 4-nitrophenyl chloroformiate in 1 ml dichloromethane is added dropwise. The mixture is stirred for 10 min at 0° C. and for additional 30 min at room temperature. The solution is cooled again to 0° C. and 72.0 μl (660 μmol, 2.7 eq) 2-dimethylaminoethyl amine in 1 ml dichloromethane are added slowly. The mixture is allowed to warm up to room temperature over night. Water and a saturated aqueous solution of sodium carbonate are added and the aqueous layer is extracted with dichloromethane. The combined organic layers are dried with magnesium sulphate and the solvent is removed under reduced pressure (210 mg crude intermediate).

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