Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930656Generated: October 27, 2026

N-Ethyltetrahydrofurfurylamine → tert-Butyl 4-(ethyl((tetrahydrofuran-2-yl)methyl)amino)-2-(4-(2-methyl-1H-imidazol-1-yl)phenylamino)-7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylate

https://huagongshe.com/reaction/1930656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-EthyltetrahydrofurfurylamineHCID 98295—
Reactanttert-Butyl 2-(4-(2-methyl-1H-imidazol-1-yl)phenylamino)-4-(trifluoromethylsulfonyloxy)-7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylateHCID 59333780—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 4-(ethyl((tetrahydrofuran-2-yl)methyl)amino)-2-(4-(2-methyl-1H-imidazol-1-yl)phenylamino)-7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylateHCID 59333772—

Reaction Conditions

Temperature85 °C

Reaction Steps

tert-Butyl 2-(4-(2-methyl-1H- imidazol-1-yl)phenylamino)-4-(trifluoromethylsulfonyloxy)-7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylate (250 mg, 0.45 mmol, example 69c) was dissolved in DMF (2 mL). N-((tetrahydrofuran-2-yl)methyl)ethanamine (58.2 mg, 0.45 mmol) was added and the reaction mixture was stirred at 85° C. overnight. The reaction was allowed to reach room temperature, the solvent was evaporated under reduced pressure and the crude was used as such in the subsequent step. MS (ES+) m/z 534.4 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188101B2
Source datasetuspto-grants-2012_05
ORD IDord-25c008e5f159425fb54c3094a57ea57d
Source noteuspto-grants-2012_05