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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 62668Erstellt: 24. Oktober 2026

Diisopropylethylamine → tert-butyl (2-(tetrahydro-2H-pyran-4-carboxamido)-4-(thiophen-2-yl)phenyl)carbamate

https://huagongshe.com/de/reaction/62668

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktOxane-4-carboxylic acidHCID 219302—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Edukttert-Butyl (2-amino-4-(thiophen-2-yl)phenyl)carbamateHCID 57717474—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkttert-butyl (2-(tetrahydro-2H-pyran-4-carboxamido)-4-(thiophen-2-yl)phenyl)carbamateHCID 7100731278,2%

Reaktionsschritte

A solution of tert-butyl (2-amino-4-(thiophen-2-yl)phenyl)carbamate (1.2 g, 4.13 mmol, 1.0 eq.), tetrahydro-2H-pyran-4-carboxylic acid (0.65 g, 4.96 mmol, 1.2 eq.), HATU (3.14 g, 8.27 mmol, 2.0 eq.) and Hünigs base (1.80 mL, 10.33 mmol, 2.5 eq.) in DMF (15 mL) was stirred for 18 h at room temperature. The reaction mixture was diluted with water. The solid was isolated by filtration and washed with hexanes to afford tert-butyl (2-(tetrahydro-2H-pyran-4-carboxamido)-4-(thiophen-2-yl)phenyl)carbamate (1.3 g, 78% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09447030B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-cdc821ed66804ad7a4e90c57cac42816
Quellennotizuspto-grants-2016_09