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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 445282Erstellt: 24. Oktober 2026

(R)-1-(4-(trifluoromethyl)phenyl)-1,2,3,4-tetrahydroisoquinoline → (R)-N-(Pyrimidin-5-yl)-1-(4-(trifluoromethyl)phenyl)-3,4-dihydroisoquinoline-2(1H)-carboxamide

https://huagongshe.com/de/reaction/445282

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(R)-1-(4-(trifluoromethyl)phenyl)-1,2,3,4-tetrahydroisoquinolineHCID 28293305—
Edukt4-Nitrophenyl pyrimidin-5-ylcarbamateHCID 59536323—
LösungsmittelAcetonitrileHCID 6342—
Produkt(R)-N-(Pyrimidin-5-yl)-1-(4-(trifluoromethyl)phenyl)-3,4-dihydroisoquinoline-2(1H)-carboxamideHCID 59536328—

Reaktionsschritte

A solution of (R)-1-(4-(trifluoromethyl)phenyl)-1,2,3,4-tetrahydroisoquinoline (100 mg, 0.30 mmol, example 30 (step 1)) and 4-nitrophenyl pyrimidin-5-ylcarbamate (93.8 mg, 0.36 mmol) in MeCN (3 mL) was heated to 70° C. overnight, and then was subjected to microwave irradiation at 120° C. for 15 min. The mixture was filtered and the filtrate was purified by preparative HPLC (0%-100% MeCN 0.1% TFA/H2O 0.1% TFA) to give the title compound in solution of H2O (0.1% TFA) and MeCN (0.1% TFA). The solvent was partially removed and saturated NaHCO3 (10 mL) was added. The mixture was extracted with EtOAc (2×5 mL). The combined organic extracts were dried over MgSO4, concentrated, and dried in vacuo to give the title compound as a light yellow solid. MS (ESI, positive ion) m/z: 399 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08476297B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-9fd39a58d785415fb0912f206d8b3213
Quellennotizuspto-grants-2013_07