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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956513Generated: October 28, 2026

Tryptamine → Diisopropylethylamine

https://huagongshe.com/reaction/1956513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTryptamineHCID 1150—
ReactantChloroformHCID 6212—
ReactantDichloromethaneHCID 6344—
ReactantTetrahydrofuranHCID 8028—
SolventPyridineHCID 1049—
SolventDiethyl EtherHCID 3283—
SolventTriethylamineHCID 8471—
ProductDiisopropylethylamineHCID 81531—

Reaction Steps

As shown in reaction Scheme B, the 2-aryltr-yptamnine may be condensed with a carboxylic acid of type (6) using the coupling reagent 1-(3 -dimethylaminopropyl)-3-ethylcarboduimide hydrochloride (EDC), 1,3-dicyclohexylcarbodiimide (DCC) or the like with or without 1-hydroxybenzotriazole (HOBt) and a tertiary amine base such as N-methylmorpholine (NMM), triethylamine or the like in an inert organic solvent such as methylene chloride, chloroform, dimethylformnamide, or mixtures thereof at or near room temperature for a period of 3-24 hours to provide the corresponding amide derivative (7). Alternatively, 2-aryltryptamine (5) can be treated with an active ester or acid chloride of type (8) in an inert organic solvent such as methylene chloride, chloroform, tetrahydrofuran, diethyl ether, or the like and a tertiary amine base such as triethylamine, diisopropylethylamine, pyridine or the like at a temperature of 0°-25° C. for 30 minutes to 4 hours to give (7). ##STR9##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780437
Source datasetuspto-grants-1998_07
ORD IDord-de64b6a614574618b4ff35767ac949c6
Source noteuspto-grants-1998_07