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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364062Generated: October 29, 2026

Potassium tert-butoxide → tert-butyl 3-benzyloxy-10,11-dihydropyrazino[1',2':1,2]imidazo[4,5-c]quinoline-9(8H)-carboxylate

https://huagongshe.com/reaction/1364062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 66958446HCID 66958446—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl 3-benzyloxy-10,11-dihydropyrazino[1',2':1,2]imidazo[4,5-c]quinoline-9(8H)-carboxylateHCID 6695845496.1%

Reaction Steps

The method described in Part D of Example 365 was used to treat tert-butyl 2-[7-benzyloxy-2-(chloromethyl)-1H-imidazo[4,5-c]quinolin-1-yl]ethylcarbamate (23.55 g, 50.43 mmol) with potassium tert-butoxide (55.47 mL of a 1 M solution in THF) with the modification that crude product mixture was purified by normal phase prep HPLC on silica gel (eluting with 2 N ammonia in methanol/chloroform in a 66-minute gradient from 0:100 to 7:93) to provide 20.87 g of tert-butyl 3-benzyloxy-10,11-dihydropyrazino[1′,2′:1,2]imidazo[4,5-c]quinoline-9(8H)-carboxylate. Material from a different run was used in Part I.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888349B2
Source datasetuspto-grants-2011_02
ORD IDord-cb3bb6491f244def880a9cc9549f8541
Source noteuspto-grants-2011_02