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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545411Generated: October 27, 2026

((R)-1-Piperidin-4-yl-pyrrolidin-2-yl)-methanol di-hydrochloride → [4-((S)-2-Hydroxymethyl-pyrrolidin-1-yl)-piperidin-1-yl]-[5-iodo-3-methyl-2-(3-trifluoromethoxy-phenyl)-3H-imidazol-4-yl]-methanone

https://huagongshe.com/reaction/545411

Reaction equation

Participants

RoleNameHCIDCharge
Reactant((R)-1-Piperidin-4-yl-pyrrolidin-2-yl)-methanol di-hydrochlorideHCID 67133026—
Reactant5-iodo-3-methyl-2-(3-trifluoromethoxy-phenyl)-3H-imidazole-4-carboxylic acidHCID 67133255—
Product[4-((S)-2-Hydroxymethyl-pyrrolidin-1-yl)-piperidin-1-yl]-[5-iodo-3-methyl-2-(3-trifluoromethoxy-phenyl)-3H-imidazol-4-yl]-methanoneHCID 57541109—

Reaction Steps

In analogy to the procedure described for example 2, 5-iodo-3-methyl-2-(3-trifluoromethoxy-phenyl)-3H-imidazole-4-carboxylic acid (example 19) and ((S)-1-piperidin-4-yl-pyrrolidin-2-yl)-methanol di-hydrochloride [prepared as described for ((R)-1-piperidin-4-yl-pyrrolidin-2-yl)-methanol di-hydrochloride (intermediate 2), but starting from (S)-(−)-pyrrolidin-2-yl-methanol] gave the title compound as brown amorphous solid. MS: 579.1 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935707B2
Source datasetuspto-grants-2011_05
ORD IDord-32df5bcc465641978f048e4b7d097113
Source noteuspto-grants-2011_05