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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675231Generated: October 30, 2026

Pyridine → (1R)-N-(1-{4-[3-chloro-4-(pyridin-2-ylmethoxy)-phenylamino]-7-(2-methoxy-ethoxy)-quinazolin-6-ylcarbamoyl}-ethyl)-acrylamide

https://huagongshe.com/reaction/1675231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcrylic AcidHCID 6581—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 67333476HCID 67333476—
SolventTetrahydrofuranHCID 8028—
Product(1R)-N-(1-{4-[3-chloro-4-(pyridin-2-ylmethoxy)-phenylamino]-7-(2-methoxy-ethoxy)-quinazolin-6-ylcarbamoyl}-ethyl)-acrylamideHCID 6733550528%

Reaction Conditions

Temperature0 °C

Reaction Steps

75 μl of acrylic acid was dissolved in 4 ml of THF, and cooled to 0° C. 180 μl of pyridine and 520 ml of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride were added thereto, the resulting solution was reacted with 284 mg of 2-amino-N-[4-[3-chloro-4-(pyridin-2-ylmethoxy)-phenylamino]-7-(2-methoxy-ethoxy)-quinazolin-6-yl]-propionamide dissolved in 4 ml of THF as a starting material for 30 mins, and then stirred for 3 hours while heating to room temperature. The reacted solution was washed with saturated sodium bicarbonate solution, extracted with a mixture of chloroform and methanol, dried over sodium sulfate, filtered and distilled under a reduced pressure, and the resulting residue was subjected to column chromatography (eluent-chloroform:methanol=15:1) to obtain the title compound (87 mg, 28%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003658B2
Source datasetuspto-grants-2011_08
ORD IDord-d346f87d600c4515ad48790a96e5f36c
Source noteuspto-grants-2011_08