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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507470Generated: November 3, 2026

Triethylamine → HCID 10832923, compound

https://huagongshe.com/reaction/507470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
Reactant7-Amino-4-[(3-bromophenyl)amino]pyrido[4,3-d]pyrimidineHCID 382059—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
ProductHCID 10832923HCID 108329237%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a stirred solution of 7-amino-4-[(3-bromophenyl)amino]pyrido[4,3-d]pyrimidine (J Med Chem, 1995;38:3780) (140 mg, 0.46 mmol), DMAP (14 mg) and Et3N (excess, 2.0 mL) at 0° C. under N2 was added acryloyl chloride (4.8 mol eq., 182 μL) dropwise over 4 hours. The reaction was then stirred at 20° C. diluted with water and extracted with EtOAc. The combined organic extracts were washed with brine, dried over anhydrous Na2SO4 and concentrated under reduced pressure before being chromatographed on silica gel eluting with MeOH/CH2Cl2/EtOAc (5:45:50), to give N-[4-[(3-bromophenyl)amino]pyrido[4,3-d]pyrimidin-7-yl]-acrylamide (12 mg, 7%) as a cream powder, mp (CH2Cl2/hexane) 215-220° C. (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786131B2
Source datasetuspto-grants-2010_08
ORD IDord-f0b9b1b0ce664cc5beec72bf0d26467c
Source noteuspto-grants-2010_08