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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972129Generated: October 29, 2026

Methyl chloroformate → HCID 86669802, compound

https://huagongshe.com/reaction/1972129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantTriethylamineHCID 8471—
ReactantHCID 67022710HCID 67022710—
SolventDichloromethaneHCID 6344—
ProductHCID 86669802HCID 8666980215.5%

Reaction Steps

To a solution (4R,10R)-4,10-diphenyl-4,5,6,8,9,10-hexahydropyrido[3,2,1-de][1,5]naphthyridin-2-amine (Intermediate 4), (110 mg, 0.322 mmol) in dichloromethane (10 mL) was added two equivalent of triethyl amine (0.090 mL, 0.644 mmol), followed by methyl chloroformate (0.037 mL, 0.483 mmol) under argon at 0° C. The reaction mixture was then stirred at room temperature for overnight. The mixture was quenched with water (30 mL). The residue was isolated in a typical aqueous workup and purified by MPLC (medium pressure liquid chromatography) using silica gel column with 10 to 15% EtOAc:Hexane to give methyl (4R,10R)-4,10-diphenyl-4,5,6,8,9,10-hexahydropyrido[3,2,1-de][1,5]naphthyridin-2-ylcarbamate, (179), (20 mg). 1H NMR (300 MHz, CDCl3) δ ppm 2.00-2.18 (m, 2H) 2.22-2.39 (m, 2H) 3.03-3.22 (m, 4H) 3.50-3.64 (m, 3H) 3.54-3.65 (m, 3H) 4.05-4.23 (m, 2H) 6.61 (br. s., 2H) 7.08-7.38 (m, 10H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431702B2
Source datasetuspto-grants-2013_04
ORD IDord-0adf57e2e4f24f28aed709812a2621de
Source noteuspto-grants-2013_04