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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20941Erstellt: 23. Oktober 2026

N-Methylbutylamine → 3-(Butyl(methyl)carbamoyl)benzoic acid

https://huagongshe.com/de/reaction/20941

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-MethylbutylamineHCID 8068—
EduktDiisopropylethylamineHCID 81531—
Edukt3-(Methoxycarbonyl)benzoic acidHCID 601880—
EduktN-Boc-cis-4-hydroxy-D-prolineHCID 688616—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
EduktMethyl 3-(butyl(methyl)carbamoyl)benzoateHCID 67316285—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-(Butyl(methyl)carbamoyl)benzoic acidHCID 43452775—

Reaktionsschritte

Step F (1): Methyl 3-(butyl(methyl)carbamoyl)benzoate. To a solution of 3-(methoxycarbonyl)benzoic acid (1.8 g, 10 mmol) in dichloromethane (40 mL) and DMF (20 mL) was added Hunig's base (2.58 g, 20 mmol) to make a clear solution and HATU (4.18 g, 11 mmol) was then added. After stirring for 10 min, the reaction mixture was added methylbutylamine (1.13 g, 13 mmol) and the reaction mixture was stirred at rt for 3 h. Dichloromethane was removed and ethyl acetate (300 mL) was added and the mixture was washed with 1N HCl, sodium carbonate solution, H2O, dried and concentrated to give the title compound ready for next step without purification: 1H NMR (CDCl3, 500 MHz) δ 0.79-0.98 (3H, m), 1.15 (1H, m), 1.41 (1H, brd s), 1.52 (1H, brd s), 1.64 (1H, m), 2.92-3.07 (2H, m), 3.21 (1H, brd s), 3.53 (1H, brd s), 3.91 (3H, s), 7.47 (1H, m), 7.58 (1H, d, J=10 Hz), 8.05-8.07 (2H, m).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745470B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-f25d641a01ff4f0589ae2ceffe2cc078
Quellennotizuspto-grants-2010_06