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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 218726Erstellt: 25. Oktober 2026

2-(Chloromethyl)-5-methylpyridine → 5-benzyloxy-N-(6-isopropylpyridin-3-yl)-N-({1-[(5-methylpyridin-2-yl)methyl)pyrazol-4-yl}methyl)-1,2,3,4-tetrahydronaphthalene-1-carboxamide

https://huagongshe.com/reaction/218726

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(Chloromethyl)-5-methylpyridineHCID 588056—
Edukt5-benzyloxy-N-(6-isopropylpyridin-3-yl)-N-[(pyrazol-4-yl)methyl]-1,2,3,4-tetrahydronaphthalene-1-carboxamide hydrochlorideHCID 67183027—
Produkt5-benzyloxy-N-(6-isopropylpyridin-3-yl)-N-({1-[(5-methylpyridin-2-yl)methyl)pyrazol-4-yl}methyl)-1,2,3,4-tetrahydronaphthalene-1-carboxamideHCID 5959719680,4%

Reaktionsschritte

By the reaction and treatment in the same manner as in Example 271 using 5-benzyloxy-N-(6-isopropylpyridin-3-yl)-N-[(pyrazol-4-yl)methyl]-1,2,3,4-tetrahydronaphthalene-1-carboxamide hydrochloride (0.78 g) and 2-(chloromethyl)-5-methylpyridine (0.43 g) as starting materials, 5-benzyloxy-N-(6-isopropylpyridin-3-yl)-N-({1-[(5-methylpyridin-2-yl)methyl]pyrazol-4-yl}methyl)-1,2,3,4-tetrahydronaphthalene-1-carboxamide (0.71 g) was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08198454B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-c61bcf37671842fdbf361e11c1e885cb
Quellennotizuspto-grants-2012_06