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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 41103Erstellt: 24. Oktober 2026

Acetic Acid → (R)-tert-butyl 2-((2-amino-4-methylphenylamino)methyl)morpholine-4-carboxylate

https://huagongshe.com/de/reaction/41103

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktDiisopropylethylamineHCID 81531—
Edukt4-Fluoro-3-nitrotolueneHCID 136287—
Edukt(R)-2-Aminomethyl-4-Boc-morpholineHCID 1515269—
KatalysatorZincHCID 23994—
LösungsmittelMethanolHCID 887—
Produkt(R)-tert-butyl 2-((2-amino-4-methylphenylamino)methyl)morpholine-4-carboxylateHCID 6717027899,6%

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

A mixture of (R)-tert-butyl 2-(aminomethyl)morpholine-4-carboxylate (0.715 g, 3.31 mmol), DIPEA (0.577 mL, 3.31 mmol), and 1-fluoro-4-methyl-2-nitrobenzene (0.513 g, 3.31 mmol) in MeOH (14 mL) was heated at 140° C. in A microwave reactor for 30 min and then cooled to room temperature. Acetic acid (1.9 mL, 33.1 mmol) was added, followed by zinc (2.162 g, 33.1 mmol). The resulting mixture was stirred at room temperature for 90 min to afford the (R)-tert-butyl 2-((2-amino-4-methylphenylamino)methyl)morpholine-4-carboxylate product (1.06 g), which was used without further purification in the next step. The product was analyzed on analytical HPLC MS using the high pH gradient method (mobile phase: 5-95% B; A: H2O with 10 mM NH4CO3 and 0.375% NH4OH v/v; B: CH3CN; 2.25 min run; X-Bridge C18; column size: 2.1×30 mm; and particle size: 5 μm). MS m/z 322.4 [M+H]+ (ESI), Rt 1.80 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08530467B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-48826e0ef53c44c2b9ad5f3907d5d719
Quellennotizuspto-grants-2013_09