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HRID 243338Erstellt: 25. Oktober 2026

N,N-Diisopropylmethylamine → (S)-1-methyl-N-(1-(1-phenyl-1H-benzo[d]imidazol-2-yl)ethyl)-1H-pyrazolo[4,3-d]pyrimidin-5-amine

https://huagongshe.com/reaction/243338

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N-DiisopropylmethylamineHCID 547370—
Edukt(S)-1-(1-Phenyl-1H-benzo[D]imidazol-2-YL)ethanamineHCID 68157455—
EduktHCID 71743115HCID 71743115—
Lösungsmittel1-ButanolHCID 263—
Produkt(S)-1-methyl-N-(1-(1-phenyl-1H-benzo[d]imidazol-2-yl)ethyl)-1H-pyrazolo[4,3-d]pyrimidin-5-amineHCID 6815728135,9%

Reaktionsschritte

A solution of (S)-1-(1-phenyl-1H-benzo[d]imidazol-2-yl)ethanamine from Example 4 (200 mg, 0.83 mmol, 1.00 equiv, 98%), 5-chloro-1-methyl-1H-pyrazolo[4,3-d]pyrimidine (180 mg, 1.07 mmol, 1.29 equiv) and methylbis(propan-2-yl)amine (0.3 mL, 98%) in n-butanol (8 mL) was stirred at 130° C. for 96 h. The resulting mixture was concentrated under vacuum and the residue was purified on a C18 column eluted with water/acetonitrile to give 110 mg (31%) of 159 as a light yellow solid. LC-MS: (ES, m/z) 370 [M+H]+, 221, 115. H-NMR: (CD3OD, 300 Hz, ppm) δ 8.86 (s, 1H), 7.70 (s, 1H), 7.65-7.54 (m, 6H), 7.61 (d, 2H), 7.09 (s, 1H), 5.30 (m, 1H), 4.04 (s, 3H), 1.64 (d, 3H)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08653089B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-f9003da174fb4f9e8742a63982d0cd83
Quellennotizuspto-grants-2014_02