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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267547Generated: November 2, 2026

Ethylamine → 3-(1-{[3-(dimethylamino)propyl]sulfonyl}-4-piperidinyl)-5-{3-[(ethylamino) methyl]phenyl}-1H-indole-7-carboxamide

https://huagongshe.com/reaction/2267547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
Reactant3-(1-{[3-(dimethylamino)propyl]sulfonyl}-4-piperidinyl)-5-(3-formylphenyl)-1H-indole-7-carboxamideHCID 59003355—
SolventDichloromethane methanolHCID 21226129—
Product3-(1-{[3-(dimethylamino)propyl]sulfonyl}-4-piperidinyl)-5-{3-[(ethylamino) methyl]phenyl}-1H-indole-7-carboxamideHCID 5900330552%

Reaction Steps

To a solution of 3-(1-{[3-(dimethylamino)propyl]sulfonyl}-4-piperidinyl)-5-(3-formylphenyl)-1H-indole-7-carboxamide (25 mg, 0.05 mmol) in MeOH/CH2Cl2 (1 mL/1 mL) was added 2M ethyl amine in THF (0.15 mL, 0.30 mmol). The reaction mixture was stirred at room temperature for 2 hours before NaBH4 (12 mg, 0.3 mmol) was added. The reaction mixture was stirred at room temperature overnight and evaporated all the solvent. The residue was purified by using a Gilson semi-preparative HPLC system, eluting with 10% B to 80% B, where A=H2O (0.1% trifluoroacetic acid) and B=CH3CN (0.1% trifluoroacetic acid) pumped at 25 mL/min to give the title compound (11 mg, 52%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858796B2
Source datasetuspto-grants-2010_12
ORD IDord-29c20d64a8d94fc9bd1af1c9bc018a14
Source noteuspto-grants-2010_12