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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258681Generated: November 2, 2026

O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate → N-{2,4-Dichloro-3-[5-chloro-1-methyl-6-(3-trifluoromethyl-piperidin-1-yl)-1H-benzimidazol-2-ylamino]-benzyl}-1-trifluoromethyl-cyclobutanecarboxamide

https://huagongshe.com/reaction/1258681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant1-(Trifluoromethyl)cyclobutanecarboxylic acidHCID 2782838—
Reactant2,4-Dichloro-3-[5-chloro-1-methyl-6-(3-(trifluoromethyl)piperidin-1-yl)-1H-benzimidazol-2-ylamino]benzylamineHCID 86674335—
SolventDimethylformamideHCID 6228—
ProductN-{2,4-Dichloro-3-[5-chloro-1-methyl-6-(3-trifluoromethyl-piperidin-1-yl)-1H-benzimidazol-2-ylamino]-benzyl}-1-trifluoromethyl-cyclobutanecarboxamideHCID 88538224—

Reaction Steps

The title compound was prepared from TBTU (35 mg, 0.11 mmol), TEA (50 μL, 0.36 mmol), 1-trifluormethyl-cyclobutanecarboxylic acid (57 mg, 0.4 mmol) and 2,4-dichloro-3-[5-chloro-1-methyl-6-(3-(trifluoromethyl)piperidin-1-yl)-1H-benzimidazol-2-ylamino]benzylamine (45.3 mg, 0.1 mmol) in DMF (3 mL) analogy to example 1 step (i).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466186B2
Source datasetuspto-grants-2013_06
ORD IDord-6d323e32c57a4a44871d44b75eb86c4c
Source noteuspto-grants-2013_06