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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40123Generated: October 26, 2026

3-Oxotetrahydrofuran → 1-Benzyl-N-(3,4-difluorobenzyl)-2-isopropyl-6-(tetrahydrofuran-3-ylamino)-1H-indole-3-carboxamide

https://huagongshe.com/reaction/40123

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-OxotetrahydrofuranHCID 529392—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant6-Amino-1-benzyl-N-(3,4-difluorobenzyl)-2-isopropyl-1H-indole-3-carboxamideHCID 59762431—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product1-Benzyl-N-(3,4-difluorobenzyl)-2-isopropyl-6-(tetrahydrofuran-3-ylamino)-1H-indole-3-carboxamideHCID 59762344—

Reaction Steps

General Procedure T. To a solution of 6-amino-1-benzyl-N-(3,4-difluorobenzyl)-2-isopropyl-1H-indole-3-carboxamide (Compound 125, 15 mg, 0.035 mmol) in MeOH (1 ml) was added dihydrofuran-3(2H)-one (Compound 129, 6.0 mg, 0.069 mmol), NaBH3CN (2.2 mg, 0.035 mmol), and HOAc (1 drop). The reaction was stirred at room temperature for 3 h, diluted with EtOAc, washed with aqueous Na2CO3 and brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified by chromatography on silica gel (0→50% EtOAc-hexanes) to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524917B2
Source datasetuspto-grants-2013_09
ORD IDord-eb0d5f0cd56b499c85be4bc1524d9cd9
Source noteuspto-grants-2013_09