تفاعل #635100

معادلة التفاعل

KOtert-Bu

dicyclohexyl-(2′,4′,6′-triisopropyl-biphenyl-2-yl)-phosphane

4-(5-bromo-pyrimidin-2-yl)-morpholine

4-amino-piperidine-1-carboxylic acid tert-butyl ester

X-Phos

→

title compound

المردود 2.0%

4-(2-Morpholin-4-yl-pyrimidin-5-ylamino)-piperidine-1-carboxylic acid tert-butyl ester

المردود 2.0%

المذيبات

toluene

ظروف التفاعل

المعالجة

1. 1
   درجة الحرارةcooled to rt
2. 2
   ترشيحfiltered
3. 3
   تركيزthe filtrate concentrated by evaporation under reduced pressure
4. 4
   أخرىThe crude material was purified with silica column chromatography
5. 5
   غسيلeluting with a gradient of heptane/ethyl acetate (3:2→2:3)

الإجراء التجريبي

To a degassed solution of 4-(5-bromo-pyrimidin-2-yl)-morpholine (4.70 g, 19.26 mmol, 1.0 equiv; commercially available) and 4-amino-piperidine-1-carboxylic acid tert-butyl ester (4.63 g, 23.11 mmol, 1.2 equiv; commercially available) in toluene (40 mL) was added KOtert-Bu (5.40 g, 48.15 mmol, 2.5 equiv), dicyclohexyl-(2′,4′,6′-triisopropyl-biphenyl-2-yl)-phosphane (0.18 g, 0.39 mmol, 0.02 equiv; X-Phos ligand [CAS RN 564483-18-7]; commercially available from Strem Chemicals, USA) and tris(dibenzylideneacetone)dipalladium(0) (1.60 g, 1.54 mmol, 0.08 equiv). The reaction mixture was stirred under nitrogen at 100° C. for 16 h, cooled to rt, filtered and the filtrate concentrated by evaporation under reduced pressure. The crude material was purified with silica column chromatography eluting with a gradient of heptane/ethyl acetate (3:2→2:3) to provide 0.14 g (2%) of the title compound in 90% purity according to 1H NMR. 1H NMR (360 MHz, DMSO): δ 1.11-1.25 (m, 2H), 1.39 (s, 9H), 1.84 (d, J=14.1 Hz, 2H), 2.88 (br s, 2H), 3.30 (br s, 1H), 3.46 (t, J=5.0 Hz, 4H), 3.64 (t, J=4.1 Hz, 4H), 3.84 (d, J=12.7 Hz, 2H), 5.03 (d, J=8.6 Hz, 1H), 7.96 (s, 2H). MS (ESI): 364.3 [M+H]+.

المصدر