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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363159Generated: November 3, 2026

5-Trifluoromethyl-1H-benzimidazole → HCID 59727095, compound

https://huagongshe.com/reaction/1363159

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Trifluoromethyl-1H-benzimidazoleHCID 349444—
ReactantHCID 59727106HCID 59727106—
ReactantHCID 59727130HCID 59727130—
ProductHCID 59727095HCID 59727095—

Reaction Steps

9-((R)-8-Fluorochroman-4-yl)-2-(6-(trifluoromethyl)-1H-benzo[d]imidazol-1-yl)-7H-purin-8(9H)-one and 9-((R)-8-fluorochroman-4-yl)-2-(5-(trifluoromethyl)-1H-benzo[d]imidazol-1-yl)-7H-purin-8(9H)-one. The title compound was synthesized from 5-trifluoromethylbenzimidazole (US 2004/0087601) via the procedures described in Example 25. Purification by column chromatography (2% MeOH/DCM) eluted the 6-trifluoromethyl isomer first (1H-NMR (300 MHz, CDCl3) δ 8.8 (d, 2H), 8.4 (s, 1H), 7.9 (d, 1H), 7.6 (d, 2H), 7.0 (t, 1H), 6.7 (m, 2H), 5.9 (t, 1H), 4.7 (m, 1H), 4.4 (m, 1H), 3.0 (m, 1H), 2.4 (m, 1H).) followed by the 5-trifluoromethyl isomer (1H-NMR (300 MHz, CDCl3) δ 9.0 (s, 1H), 8.4 (s, 1H), 8.1 (s, 1H), 8.0 (d, 1H), 7.6 (d, 2H), 7.0 (m, 1H), 6.8 (m, 2H), 5.9 (t, 1H), 4.7 (m, 1H), 4.4 (m, 1H), 2.9 (m, 1H), 2.4 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884109B2
Source datasetuspto-grants-2011_02
ORD IDord-c0fcbb3d7f2940f991cfab08a40d46c4
Source noteuspto-grants-2011_02