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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275132Generated: November 2, 2026

4-Methylmorpholine → Methyl 4-[6-(cyclopentyloxycarbonyl) amino-2,3-dihydrobenz-1,4-oxazin-4-ylmethyl]-3-methoxybenzoate

https://huagongshe.com/reaction/275132

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantCyclopentyl chloroformateHCID 2735892—
ReactantMethyl 4-(6-amino-2,3-dihydrobenz-1,4-oxazin4-ylmethyl)-3-methoxybenzoateHCID 14763126—
SolventDichloromethaneHCID 6344—
ProductMethyl 4-[6-(cyclopentyloxycarbonyl) amino-2,3-dihydrobenz-1,4-oxazin-4-ylmethyl]-3-methoxybenzoateHCID 1476312752.2%

Reaction Steps

Cyclopentyl chloroformate (0.5 g.) was added in a single portion to a stirred solution of methyl 4-(6-amino-2,3-dihydrobenz-1,4-oxazin-4-ylmethyl)-3-methoxybenzoate (L) (1.0 g.) and N-methylmorpholine (0.314 g.) in dichloromethane (30 ml.), under an atmosphere of nitrogen. After one hour, the mixture was diluted with dichloromethane and washed successively with 1M hydrochloric acid, 5% w/v sodium bicarbonate solution, and saturated brine, then dried (MgSO4) and evaporated. The residue was purified by flash chromatography on silica gel (4 cm. diameter column), eluting with dichloromethane to give the title compound (0.7 g, 52%) as an oil; NMR (80 MHz, CDCl3): 1.69[m,8H, (CH2)4 ], 3.39(t,2H, OCH2CH2N), 3.90(s,3H, OCH3), 3.91(s,3H, OCH3), 4.23(t,2H, OCH2CH2N), 4.45(s,2H, CH2.Ar), 5.10(m,1H, --CHO--), 6.2(br s,1H, NHCO), 6.59-7.62(m,6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05391758
Source datasetuspto-grants-1995_02
ORD IDord-4076fc8442264224b3dca1d1b658b6f3
Source noteuspto-grants-1995_02