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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016663Generated: October 25, 2026

Triethylamine → 1-[[[(4-isothiocyanatophenyl)carbonyl]amino]butyl]-N,N-diethyl-D-lysergamide

https://huagongshe.com/reaction/1016663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Isothiocyanatobenzoyl chlorideHCID 637654—
Reactant1-(3-aminobutyl)-N,N-diethyl-D-lysergamideHCID 22894552—
SolventTetrahydrofuranHCID 8028—
Product1-[[[(4-isothiocyanatophenyl)carbonyl]amino]butyl]-N,N-diethyl-D-lysergamideHCID 2289455462.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 370 mg (0.94 mmol) of 5 in 15 mL of dry THF was cooled to 0° C. and treated with a solution of 190 mg (0.96 mmol) of 6 in 5 mL of dry THF, stirred at 0° C. for 30 minutes and then at room temperature overnight. The reaction mixture was treated with 0.14 mL (1.0 mmol) of triethylamine and stirred at room temperature for 2 hours The reaction mixture was concentrated at reduced pressure. The residue was dissolved in methylene chloride, washed with H2O, dried over anhydrous sodium sulfate and concentrated at reduced pressure. The residue was chromatographed on 200 g of silica gel using 3% methanol in methylene chloride as eluent to yield 325 mg (62%) of 7 as a tan amorphous solid [α]D=+47.5° (c=0.91%; CHCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476199B1
Source datasetuspto-grants-2002_11
ORD IDord-c7813d691e3849cc95036e9426a1ea7e
Source noteuspto-grants-2002_11