Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1777809Erstellt: 25. Oktober 2026

Dabco → HCID 118274963, Verbindung

https://huagongshe.com/reaction/1777809

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDabcoHCID 9237—
EduktAmmonium AcetateHCID 517165—
Edukt2-Chloro-1,3-bis(dimethylamino)trimethinium hexafluorophosphateHCID 10590807—
Edukt(S)-ethyl 4-(tert-butoxycarbonyl)amino-5-methyl-3-oxohexanoateHCID 13968762—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 118274963HCID 11827496351%

Reaktionsschritte

To a mixture of ethyl(S)-4-((tert-butoxycarbonyl)amino)-5-methyl-3-oxohexanoate (9.68 g, 33.7 mmol) from above in THF (100 mL) at 0° C. was added potassium tert-butoxide (3.78 g, 35.4 mmol). The mixture was warmed to rt and stirred for 45 min, at which point 1,4-diazabicyclo[2.2.2]octane (3.78 g, 33.7 mmol) and 2-chloro-1,3-bis(dimethylamino)trimethinium hexaflurophosphate (15.5 g, 50.5 mmol) were added successively. The mixture was heated to 45° C. and stirred for 3 h, at which point ammonium acetate (5.19 g, 67.4 mmol) was added. The mixture was then heated to reflux and stirred for 15 h. It was then cooled to rt and concentrated under reduced pressure. The residue was dry-loaded onto a silica gel column and purified (eluting with 5% EtOAc in hexanes, gradient to 15%) to yield 6.09 g of ethyl(S)-2-(1-((tert-butoxycarbonyl)amino)-2-methylpropyl)-5-chloronicotinate (51%). LC-MS tR=1.14 min in 1 min chromatography, MS (ESI) m/z 357.3 [M+H]+. 1H NMR (CDCl3, 400 MHz): δ 8.61 (d, J=2.4 Hz, 1H), 8.18 (d, J=2.8 Hz, 1H), 5.71 (d, J=9.6 Hz, 1H), 5.62 (dd, J=5.2 Hz, 9.6 Hz, 1H), 4.42 (q, J=7.2 Hz, 2H), 2.08-2.00 (m, 1H), 1.42 (s, 9H), 1.42 (t, J=7.2 Hz, 3H), 0.93 (d, J=6.4 Hz, 3H), 0.83 (d, J=6.4 Hz, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09266886B2
Quelldatensatzuspto-grants-2016_02
ORD IDord-42c716e7ea4048248bef4fe9ce7b465b
Quellennotizuspto-grants-2016_02