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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30813Generated: October 28, 2026

Acetic Acid → N-[4-({2-[(3-isopropylphenyl)amino]-1-methyl-1H-benzimidazol-5-yl}oxy)pyridin-2-yl]-2-(1-methylpiperidin-4-yl)acetamide

https://huagongshe.com/reaction/30813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantSodium CarbonateHCID 10340—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantN-(4-(2-(3-isopropylphenylamino)-1-methyl-1H-benzo[d]imidazol-5-yloxy)pyridin-2-yl)-2-(piperidin-4-yl)acetamideHCID 59790190—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductN-[4-({2-[(3-isopropylphenyl)amino]-1-methyl-1H-benzimidazol-5-yl}oxy)pyridin-2-yl]-2-(1-methylpiperidin-4-yl)acetamideHCID 59790284—

Reaction Steps

To the mixture containing N-(4-(2-(3-isopropylphenylamino)-1-methyl-1H-benzo[d]imidazol-5-yloxy)pyridin-2-yl)-2-(piperidin-4-yl)acetamide (1 eq), glacial acetic acid (2 eq), and formaline (7.5 eq) in tetrahydrofuran:methanol (1:1) was added sodium cyanoborohydride (2 eq) and stirred at room temperature for one hour. Reaction neutralized with saturated sodium carbonate solution and extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate and concentrated to give crude product. Purification by HPLC to yield N-[4-({2-[(3-isopropylphenyl)amino]-1-methyl-1H-benzimidazol-5-yl}oxy)pyridin-2-yl]-2-(1-methylpiperidin-4-yl)acetamide. HPLC=3.51 min; MS: MH+=513.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423150B2
Source datasetuspto-grants-2008_09
ORD IDord-d034d5bc5a394e5480b48fd4fcafef94
Source noteuspto-grants-2008_09