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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 230002Erstellt: 24. Oktober 2026

Thiophosgene → HCID 68834931, Verbindung

https://huagongshe.com/de/reaction/230002

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThiophosgeneHCID 10040—
EduktDiisopropylethylamineHCID 81531—
EduktSodium BicarbonateHCID 516892—
Edukt4-methoxy-1-N-methylbenzene-1,2-diamineHCID 4518444—
EduktMethyl 4-{[(4-tert-butylcyclohexyl)amino]methyl}benzoateHCID 16100290—
KatalysatorHg(TFA)2HCID 16685285—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 68834931HCID 68834931—

Reaktionsschritte

To a solution of the title compound of Example 1 Step B (2.5 mmol, 759 mg) and DIEA (3 mmol, 0.52 mL) in 10 mL of DCM was added thiophosgene (2.5 mmol, 0.19 mL) (exothermic). After 15 min the title compound of Example 14 Step B (3 mmol, 456 mg) and DIEA (3 mmol, 0.52 mL) were added to the solution. After 30 min Hg(O2CCF3)2 (2.5 mmol, 1.1 g) was added (exothermic), resulting in formation of an orange precipitate. After 30 min the solution was poured into NaHCO3 (aq) containing Na2S, and the slurry was filtered through celite, and the filter cake was washed with DCM. The organic phase was collected and the aqueous phase was extracted with 2×DCM. The combined organic phase was dried with Na2SO4 and concentrated under reduced pressure affording a tan solid. Purification by flash chromatography on silica eluting with 25% EtOAc/hexanes afforded the product as a white solid. 1H NMR (500 MHz, CDCl3) δ 7.92 (d, 2H), 7.45 (d, 2H), 7.20 (d, 1H), 7.08 (d, 1H), 6.84 (dd, 1H), 4.63 (s, 2H), 3.90 (s, 3H), 3.86 (s, 3H), 3.18 (m, 1H), 2.11 (m, 2H), 1.90 (m, 2H), 1.60 (m, 2H), 0.96-1.15 (overlapping m, 3H), 0.87 (s, 9H). MS (ESI): m/z 464 (M+H). HPLC A: 2.45 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07563815B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-b0f8a82db34f43edb05893ef9f0aac28
Quellennotizuspto-grants-2009_07