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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668798Generated: October 31, 2026

Methyl chloroformate → HCID 11508604, compound

https://huagongshe.com/reaction/1668798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 11471935HCID 11471935—
CatalystSodium SulfateHCID 24436—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 11508604HCID 1150860472%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (6-amino-2-methyl-quinazolin-4-yl)-(4-methoxy-phenyl)-methylamine (150 mg, 0.51 mmol) in 5 ml of THF was added potassium carbonate (160 mg, 1.16 mmol), 2 mg of sodium sulfate. The reaction mixture was cooled to 0° C., and methyl chloroformate (0.4 ml, 5 mmol) was added. The reaction mixture was stirred at 0° C. for 10-15 min, then diluted with EtOAc (20 ml), washed with water, brine, dried over Na2SO4, filtered and concentrated by vacuum. The crude product was purified by chromatography on silica gel with acetate, hexane (1:3 to 1:1) as eluent, yielding 129 mg of title compound (72%) as yellow solids. 1H NMR (CDCl3): 7.70 (s, 2H), 7.12-7.07 (m, 2H), 6.94-6.89 (m, 3H), 6.32 (brs, 1H), 3.84 (s, 3H), 3.70 (s, 3H), 3.57 (s, 3H), 2.70 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989462B2
Source datasetuspto-grants-2011_08
ORD IDord-ee00946a4d494bc3bb232704161a77c4
Source noteuspto-grants-2011_08