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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299114Generated: October 31, 2026

1-[(2-methyl-5,8-dihydro-4-quinolinyl)methyl]-1H-indole-5-carbonyl chloride → methyl {4-[({1-[(2-methyl-5,8-dihydro-4-quinolinyl)methyl]-1H-indol-5-yl}carbonyl)amino]tetrahydro-2H-pyran-4-yl}acetate

https://huagongshe.com/reaction/2299114

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[(2-methyl-5,8-dihydro-4-quinolinyl)methyl]-1H-indole-5-carbonyl chlorideHCID 22258380—
ReactantMethyl 4-aminotetrahydro-2H-pyran-4-acetateHCID 25418820—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Productmethyl {4-[({1-[(2-methyl-5,8-dihydro-4-quinolinyl)methyl]-1H-indol-5-yl}carbonyl)amino]tetrahydro-2H-pyran-4-yl}acetateHCID 8658427917.2%

Reaction Steps

The methyl (4-aminotetrahydro-2H-pyran-4-yl)acetate (0.13 g, 0.75 mmol) from example (355) was combined with the acid chloride (0.20 g, 0.49 mmol) from step (402b) in methylene chloride (15 ml) and water saturated sodium bicarbonate (15 ml). The reaction was stirred for 3.5 hs, partitioned between methylene chloride and water. The organic layer was washed with brine, dried over magnesium sulfate and concentrated to give a solid. This was purified by flash chromatography on silica gel eluting hexane: ethyl acetate (25:75, v:v) to give the methyl {4-[({1-[(2-methyl-5,8-dihydro-4-quinolinyl)methyl]-1H-indol-5-yl}carbonyl)amino]tetrahydro-2H-pyran-4-yl}acetate (0.04 g, 17%) as a solid, MS (M+H)+=472.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495565B2
Source datasetuspto-grants-2002_12
ORD IDord-feddc33fd1e047bc882d8125de088ad3
Source noteuspto-grants-2002_12