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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16181Erstellt: 24. Oktober 2026

Ammonium Chloride → trans-N-(7-Chloro-2,3,4,14b-tetrahydro12-methyl-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)-2,2,2-trifluoroacetamide

https://huagongshe.com/de/reaction/16181

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
EduktHCID 86599893HCID 86599893—
EduktHCID 178477797HCID 178477797—
KatalysatorFerrocene palladium dichlorideHCID 131728027—
LösungsmittelTetrahydrofuranHCID 8028—
Produkttrans-N-(7-Chloro-2,3,4,14b-tetrahydro12-methyl-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)-2,2,2-trifluoroacetamideHCID 86599892—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a solution of trans-N-(12-bromo-7-chloro-2,3,4,14b-tetrahydro-1H-dibenzo[b,f]pyrido-[1,2-d][1,4]oxazepin-1-yl)-2,2,2-trifluoroacetamide (80 mg, 0.17 mmol) in THF (2 mL) was added ferrocene PdCl2 (5 mg, 7 μmol), and the reaction mixture was stirred for 5 min. Methylzinc chloride was added dropwise whereafter the reaction mixture was heated to 60° C. and stirred overnight at 60° C. The mixture was poured into sat (aq) NH4Cl and extracted with ethyl acetate (3×). The combined organic layers were washed with brine, dried (Na2SO4) and evaporated. After purification on silica and with HPLC the title compound was obtained (13.2 mg, 19%). Data: 1H-NMR (400 MHz, DMSO) 1.60-1.85 (m, 3H), 2.0 (m, 1H), 2.23 (s, 3H), 3.11 (td, J=2.8, 13.2, 1H), 3.85 (d, J=14, 1H), 4.10 (d, J=10, 1H), 4.40 (m, 1H), 6.69-7.10 (6 ArH), 9.16 (d, J=10, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737136B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-74de55984cef41bc8c4b69e2239e6d49
Quellennotizuspto-grants-2010_06