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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486916Generated: October 30, 2026

Diisopropylethylamine → Ethyl 6-bromo-4-(oxan-4-ylamino)quinoline-3-carboxylate

https://huagongshe.com/reaction/1486916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-AminotetrahydropyranHCID 419223—
ReactantEthyl 6-bromo-4-chloroquinoline-3-carboxylateHCID 2764138—
SolventDimethylacetamideHCID 31374—
ProductEthyl 6-bromo-4-(oxan-4-ylamino)quinoline-3-carboxylateHCID 11849864996.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

On a larger scale, ethyl 6-bromo-4-chloroquinoline-3-carboxylate (2196 g, (1976 g active), 6.28 mol) was charged to the vessel with DMA (16 L). Tetrahydro-2H-pyran-4-amine (1224 g, 12.10 mol) was added over 10 minutes with an observed exotherm of 21-27° C. DIPEA (3.5 L, 20.09 mol) was added with no observed exotherm. The mixture was heated to 75-85° C. and the resulting solution stirred for 18.5 h at 80° C. HPLC indicated consumption of starting material and 99.2% product. The reaction was cooled to 50° C. and then poured into water (50 L). The resulting suspension was stirred for 2 h at r.t. and the solids isolated by filtration, washing with water (8 L then 2×4 L). The solid was dried under vacuum at 40° C. for 55 h to give 2307 g of desired material. Analytical data was consistent with that obtained from previous batches.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428503B2
Source datasetuspto-grants-2016_08
ORD IDord-497104888776471e99cb150086558a20
Source noteuspto-grants-2016_08