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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564223Generated: November 3, 2026

Formaldehyde → 2-(5-((2r)-1-Methylpyrrolidin-2-yl)thien-2-yl)-1h-benzimidazole-4-carboxamide

https://huagongshe.com/reaction/564223

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2-(5-((2r)-Pyrrolidin-2-yl)thien-2-yl)-1h-benzimidazole-4-carboxamideHCID 66760237—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-(5-((2r)-1-Methylpyrrolidin-2-yl)thien-2-yl)-1h-benzimidazole-4-carboxamideHCID 66758802—

Reaction Steps

A solution of EXAMPLE 16D (50 mg) in methanol (20 mL) was treated with 37 wt % formaldehyde in water (114 μL) and stirred overnight. Sodium cyanoborohydride (315 mg) was added, and the solution was stirred for 3 hours and concentrated. The concentrate was dissolved in methanol and TFA, and purified by HPLC (Zorbax C-8, 0.1% TFA/acetonitrile/water). 1H NMR (CD3OD) δ 2.30 (m, 2H), 2.47 (m, 1H), 2.74 (m, 1H), 2.94 (s, 3H), 3.31-3.40 (m, 1H), 3.88 (m, 1H), 4.81 (m, 1H), 7.40 (t, J=7.7 Hz, 1H), 7.51 (d, J=3.7 Hz, 1H), 7.73 (d, J=7.6 Hz, 1H), 7.86 (d, J=4.0 Hz, 1H), 7.95 (d, J=7.6 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067613B2
Source datasetuspto-grants-2011_11
ORD IDord-361845f7a3cd442ea76248c3db346514
Source noteuspto-grants-2011_11