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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20851Generated: October 30, 2026

[2-Methyl-1-phenyl-2-(1-pyrrolidinyl)propyl]amine → N-[2-Methyl-1-phenyl-2-(1-pyrrolidinyl)propyl]-2-(methylthio)-4,6-bis(trifluoromethyl)benzamide

https://huagongshe.com/reaction/20851

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[2-Methyl-1-phenyl-2-(1-pyrrolidinyl)propyl]amineHCID 25158607—
ReactantHCID 59347928HCID 59347928—
CatalystTriethylamineHCID 8471—
SolventDichloromethaneHCID 6344—
ProductN-[2-Methyl-1-phenyl-2-(1-pyrrolidinyl)propyl]-2-(methylthio)-4,6-bis(trifluoromethyl)benzamideHCID 5934780585%

Reaction Steps

A solution of 2-(methylthio)-4,6-bis(trifluoromethyl)benzoyl chloride D55 (60 mg; 0.19 mmol) in dry DCM (1 ml) was treated with (+)-[2-methyl-1-phenyl-2-(1-pyrrolidinyl)propyl]amine D6 (60 mg, 0.27 mmol) followed by triethylamine (5drops) and left overnight at room temperature. The volatile components were removed under reduced pressure and the residue chromatographed on silica gel. Elution with 0-80% ethyl acetate in pentane gave the title product as an oil (80 mg, 85%). 1H NMR (CDCl3) δ: 0.94 (3H, s), 1.00 (3H, s), 1.69 (4H, overlapping m), 2.54 (3H, s), 2.62 (2H, m), 2.72 (2H, m), 4.78 (1H, s), 7.25-7.45 (6H, overlapping m), 7.68 (1H, s), 7.72 (1H, s). Mass Spectrum (Electrospray LC/MS): Found 505 (MH+) C24H26F6N2OS requires 504. Ret time 2.24 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745642B2
Source datasetuspto-grants-2010_06
ORD IDord-88907c530e6d4ce8a7ff9609deb5ba75
Source noteuspto-grants-2010_06