Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582300Generated: November 1, 2026

2,3-Dihydro-1-benzofuran-7-carbaldehyde → (1H-Benzimidazol-2-ylmethyl)-(2,3-dihydro-benzofuran-7-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine

https://huagongshe.com/reaction/1582300

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dihydro-1-benzofuran-7-carbaldehydeHCID 2795018—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-[(5,6,7,8-Tetrahydroquinolin-8-ylamino)-methyl]-benzimidazole-1-carboxylic acid tert-butyl esterHCID 21985081—
Product(1H-Benzimidazol-2-ylmethyl)-(2,3-dihydro-benzofuran-7-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amineHCID 21984995—

Reaction Steps

Following General Procedure B: To a solution of 2,3-dihydrobenzofuran-7-carboxaldehyde (53.6 mg, 0.362 mmol) and [1-(tert-butoxycarbonyl)-(1H-benzimidazol-2-ylmethyl)]-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (136 mg, 0.361 mmol) CH2Cl2 (5 mL) was added NaBH(OAc)3 (112 mg, 0.528 mmol) and the mixture stirred overnight. Purification of the crude product by radial chromatography on silica gel (1 mm TLC plate, 125:1:1 CH2Cl2: CH3OH: NH4OH) to gave the desired freebase (48 mg, 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06734191B2
Source datasetuspto-grants-2004_05
ORD IDord-5e979fe7e8e1467c9b1e9ca7c246366e
Source noteuspto-grants-2004_05