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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848762Generated: October 31, 2026

4-(Trifluoromethyl)piperidine → HCID 90410206, compound

https://huagongshe.com/reaction/1848762

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)piperidineHCID 136469—
Reactant4-(Trifluoromethyl)piperidine hydrochlorideHCID 16218160—
ReactantHCID 90410891HCID 90410891—
ProductHCID 90410206HCID 90410206—

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-bromobenzyl)-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 C32H38F3N5O3, 597.29; m/z found, 598.2 [M+H]+. 1H NMR (500 MHz, CD3OD) δ 7.70 (d, J=9.1, 1H), 7.55 (d, J=2.3, 1H), 7.35 (d, J=2.3, 1H), 7.26 (dd, J=9.0, 2.3, 1H), 7.20-7.15 (m, 2H), 7.10-7.02 (m, 2H), 6.31 (d, J=2.3, 1H), 5.68 (s, 2H), 5.07 (s, 2H), 3.85 (s, 3H), 3.83-3.77 (m, 2H), 3.41 (s, 2H), 2.85 (td, J=12.6, 2.6, 2H), 2.46-2.29 (m, 1H), 2.00-1.95 (m, 2H), 1.86-1.60 (m, 6H), 0.87 (t, J=7.4, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952177B2
Source datasetuspto-grants-2015_02
ORD IDord-1146760cede44c40ac40ad7ce1166f22
Source noteuspto-grants-2015_02