Pyrrolidine → HCID 67974672, compound

HRID 1777609Notes

Reaction equation

HRID 1777609 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH:6]=[C:5]2[CH2:11][CH2:12][NH:13][C:14](=[O:23])[C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([CH2:21]Cl)[CH:16]=1.[NH:24]1[CH2:28][CH2:27][CH2:26][CH2:25]1>C1COCC1>[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH:6]=[C:5]2[CH2:11][CH2:12][NH:13][C:14](=[O:23])[C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([CH2:21][N:24]2[CH2:28][CH2:27][CH2:26][CH2:25]2)[CH:16]=1

Participants

4

Reactant 2

HCID 31268PyrrolidineHCID 67974165N-(2-(5-chloro-1H-indol-3-yl)ethyl)-3-(chloromethyl)benzamide

Product 1

HCID 67974672HCID 67974672, compoundYield 67.3%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

N-(2-(5-Chloro-1H-indol-3-yl)ethyl)-3-(pyrrolidin-1-ylmethyl)benzamide was prepared following Method C starting from N-(2-(5-chloro-1H-indol-3-yl)ethyl)-3-(chloromethyl)benzamide (0.050 g; 0.144 mmol) and pyrrolidine (0.042 mL; 0.5 mmol) in THF (3 mL), under a microwave irradiation at 150° C. for 5 minutes. Flash chromatography on silica gel (eluent 3 to 20% ethanol in dichloromethane) furnished 0.037 g (67%) of the title compound as a white solid.

Workup

  1. customN-(2-(5-Chloro-1H-indol-3-yl)ethyl)-3-(pyrrolidin-1-ylmethyl)benzamide was prepared

Sources & evidence

ORD record
ord-8f46c0eef68c45d3bb32037afd34cfc5
Source dataset
uspto-grants-2016_02
Patent number
US09266832B2

Reaction notes

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