Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733679Generated: October 27, 2026

Ethylmorpholine → HCID 57840793, compound

https://huagongshe.com/reaction/733679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylmorpholineHCID 7525—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant4-AminomethyltetrahydropyranHCID 2773210—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant7-chloro-1H-pyrrolo[2,3-c]pyridine-4-carboxylic acidHCID 57840843—
SolventDimethylformamideHCID 6228—
ProductHCID 57840793HCID 5784079356.6%

Reaction Steps

To a solution of 7-chloro-1H-pyrrolo[2,3-c]pyridine-4-carboxylic acid (110 mg) in dimethylformamide (4 ml) was added 4-ethylmorpholine (187 μl), tetrahydro-pyran-4-ylmethylamine (97 mg), 1-hydroxybenzotriazole hydrate (118 mg) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (129 mg) and the solution stirred at room temperature overnight. The dimethylformamide was evaporated and the residue dissolved in ethyl acetate (10 ml). The organic layer was then washed with 5% sodium hydrogen carbonate solution (4 ml) and brine (4 ml). The organic layer was dried (MgSO4) and evaporated to give a pale orange solid. The solid was triturated with diethyl ether and then filtered off, sucked dry then dried at 40° C. under vacuum to afford the title compound (93 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589206B2
Source datasetuspto-grants-2009_09
ORD IDord-3edbe2e917894c798517cf8153eeef79
Source noteuspto-grants-2009_09