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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378139Generated: November 3, 2026

3,5-Bis(trifluoromethyl)benzyl bromide → HCID 86613817, compound

https://huagongshe.com/reaction/2378139

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Bis(trifluoromethyl)benzyl bromideHCID 122573—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 58926753HCID 58926753—
ReactantHCID 69643684HCID 69643684—
ProductHCID 86613817HCID 8661381720%

Reaction Steps

Prepare the title compound by essentially following the procedure described in Example 49, Step 2, by replacing (+/−)-N-(1-cyclopentyl-6-methoxy-2-methyl-1,2,3,4-tetrahydro-[1,5]napthyridin-4-yl)-acetamide, with 2-ethyl-3-methyl-4-(5,6,7,8-tetrahydro-quinolin-3-ylamino)-3,4,6,7,8,9-hexahydro-2H-benzo[b][1,5]napthyridine-1-carboxylic acid isopropyl ester (0.175 g, 0.378 mmol), and using 3,5-bis trifluoromethyl benzyl bromide and lithium hexamethyldisilazide. Purify using silica gel column chromatography (gradient eluent, 50:50 ethyl acetate in hexane) to afford the title compound (0.052 g, 20%). MS (ES+): 689 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470705B2
Source datasetuspto-grants-2008_12
ORD IDord-8fa763191991478e81880f33c404c7f1
Source noteuspto-grants-2008_12