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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848761Generated: November 2, 2026

4-(Trifluoromethyl)piperidine → HCID 90411248, compound

https://huagongshe.com/reaction/1848761

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)piperidineHCID 136469—
Reactant4-(Trifluoromethyl)piperidine hydrochlorideHCID 16218160—
ReactantHCID 86269707HCID 86269707—
ProductHCID 90411248HCID 90411248—

Reaction Steps

The title compound was prepared in a manner analogous to that in Example 152 substituting 4-(trifluoromethyl)piperidine hydrochloride and 2-((1-(4-bromo-2-fluorobenzyl)-6-((1-methyl-1H-pyrazol-3-yl)methoxy)-1H-benzo[d]imidazol-2-yl)methyl)-2-ethylbutanoic acid and 4-(trifluoromethyl)piperidine. MS (ESI): mass calcd. for C32H37F4N5O3, 615.28; m/z found, 615.2 [M+H]+. 1H NMR (400 MHz, CD3OD) δ 7.68 (d, J=9.0, 1H), 7.56 (d, J=2.3, 1H), 7.40 (d, J=2.3, 1H), 7.26 (dd, J=9.0, 2.3, 1H), 7.24-7.18 (m, 1H), 6.80-6.73 (m, 2H), 6.33 (d, J=2.3, 1H), 5.68 (s, 2H), 5.09 (s, 2H), 3.88 (s, 3H), 3.87-3.84 (m, 2H), 3.46 (s, 2H), 2.80 (td, J=12.7, 2.6, 2H), 2.43-2.30 (m, 1H), 1.97-1.88 (m, 2H), 1.87-1.68 (m, 4H), 1.68-1.53 (m, 2H), 0.88 (t, J=7.4, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952177B2
Source datasetuspto-grants-2015_02
ORD IDord-3bf18b78d88a4786b7e6842ba0b2044a
Source noteuspto-grants-2015_02