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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49235Generated: October 29, 2026

Tributylamine → HCID 178448171, compound

https://huagongshe.com/reaction/49235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylamineHCID 7622—
ReactantHCID 178448172HCID 178448172—
ReactantHCID 178515977HCID 178515977—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
ProductHCID 178448171HCID 178448171—

Reaction Steps

In a sealed glass bottle under N2-atmosphere, 424 mg (2.92 mmol) of trans 2-isopropyl-[1,3]dioxan-5-ylamine, 396 mg (1.46 mmol) of 1-chloro-4-[(6-hydroxy-pyridin-3-yl)methyl]-isoquinoline (contains 1-iodo derivative) and 2 ml of tributylamine are stirred at 150° C. for 48 h. The resulting mixture is diluted with EtOAc and NaHCO3-solution, the aqueous layer is separated and extracted twice with EtOAc. The organic phases are washed with brine, dried (Na2SO4) and concentrated in vaccuo. “Reversed Phase” medium-pressure chromatography (water/acetonitrile/TFA) yields trans 1-(2-isopropyl-[1,3]dioxan-5-ylamino)-4-[(6-hydroxy-pyridin-3-yl)methyl]-isoquinoline; FAB-MS; (M+H)+=286; HPLC(gradient20-100) tRet=8.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706731B2
Source datasetuspto-grants-2004_03
ORD IDord-e9ac4aa747d3472587e973ff00ac2a98
Source noteuspto-grants-2004_03