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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 711421Erstellt: 25. Oktober 2026

Selenium Dioxide → HCID 86654702, Verbindung

https://huagongshe.com/reaction/711421

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSelenium DioxideHCID 24007—
Edukt2,4-DimethoxybenzylamineHCID 597250—
EduktSodium cyanoborohydrideHCID 5003444—
EduktMethyl 2-((1R,2S)-2-(tert-butoxycarbonylamino)cyclohexylamino)-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylateHCID 67238015—
LösungsmittelMethanolHCID 887—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktHCID 86654702HCID 8665470237%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of methyl 2-((1R,2S)-2-(tert-butoxycarbonylamino)cyclohexylamino)-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylate (500 mg, 1.065 mmol) and selenium dioxide (236 mg, 2.130 mmol) in dioxane (10 mL) was heated at 100° C. for 24 h. The solution was subsequently cooled and filtered. The filtrate was concentrated under reduced pressure and dried to give a brown foam (534 mg; dihydroxyl form was observed via mass spectroscopy), which was used directly in the next step without further purification. A mixture of the unpurified intermediate (534 mg, 1.065 mmol) and (2,4-dimethoxyphenyl)methanamine (0.160 mL, 1.065 mmol) in MeOH (10 mL) was stirred at RT for 10 min, after which sodium cyanoborohydride (100 mg, 1.597 mmol) was added, and the reaction mixture was stirred at RT for 20 h. The reaction mixture was warmed to 50° C. and stirred for an additional 2 h to complete the reaction. The mixture was cooled to RT and the solid filtered and washed with MeOH to give the title compound as a pinkish solid (237 mg, 37%). [M+H] calc'd for C33H42N6O5, 603. found, 603.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09181255B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-803a773fc4294270b2fbc7a19de2da35
Quellennotizuspto-grants-2015_11