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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245845Generated: October 30, 2026

Benzaldehyde → 2-[(Aminocarbonyl)amino]-5-[4-((3-hydroxypyrrolidin-1-yl)methyl)phenyl]thiophene-3-carboxamide

https://huagongshe.com/reaction/1245845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantTrimethyl orthoformateHCID 9005—
Reactant4-HydroxypyrrolidineHCID 98210—
ReactantCyano-borohydrideHCID 498716—
Reactant2-[(Aminocarbonyl)amino]-5-[4-formylphenyl]thiophene-3-carboxamideHCID 21914326—
SolventAcetic AcidHCID 176—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventDimethylacetamideHCID 31374—
Product2-[(Aminocarbonyl)amino]-5-[4-((3-hydroxypyrrolidin-1-yl)methyl)phenyl]thiophene-3-carboxamideHCID 2191430324.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-[(Aminocarbonyl)amino]-5-(4-formylphenyl)-3-thiophenecarboxamide (100 mg) was stirred in a mixture of 1,2-dimethoxyethane (10 ml) and N,N-dimethylacetamide (5 ml). 3-pyrrolidinol (0.15 g) was added, followed by trimethyl orthoformate (5 ml) and acetic acid (0.5 ml). The reaction was stirred at 80° C. for 20 minutes, and then polymer-supported cyanoborohydride (0.45 g) was added. The reaction was stirred at 80° C. for a further 2 h, and then polymer-supported benzaldehyde (0.5 g) was added. The resins were removed by filtration, and the filtrate was then passed through a 5 g SCX column, washing with methanol (25 ml). The product was eluted using 1M methanolic ammonia (45 ml), and this solution was then evaporated to dryness under reduced pressure. Purification by chromatography on silica, eluting with dichloromethane/methanol (9:1), gave the product as an off-white solid (30 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125896B2
Source datasetuspto-grants-2006_10
ORD IDord-2f96afb09b514276b2ae710c19aa6b47
Source noteuspto-grants-2006_10