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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acrylic Acid | HCID 6581 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 67333476 | HCID 67333476 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1R)-N-(1-{4-[3-chloro-4-(pyridin-2-ylmethoxy)-phenylamino]-7-(2-methoxy-ethoxy)-quinazolin-6-ylcarbamoyl}-ethyl)-acrylamide | HCID 67335505 | 28% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08003658B2 |
|---|
| Source dataset | uspto-grants-2011_08 |
|---|
| ORD ID | ord-d346f87d600c4515ad48790a96e5f36c |
|---|
| Source note | uspto-grants-2011_08 |
|---|