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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656591Generated: October 30, 2026

HCID 45257321, compound → HCID 178501345, compound

https://huagongshe.com/reaction/656591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 45257321HCID 45257321—
Reactant(2S,4R)-1-tert-butyl 2-methyl 4-(aminooxy)pyrrolidine-1,2-dicarboxylateHCID 57999148—
CatalystDiacetyloxymercuryHCID 16683746—
SolventTolueneHCID 1140—
ProductHCID 178501345HCID 178501345570%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of (R)-2-amino-7-(2-bromo-4-fluorophenyl)-4-methyl-7,8-dihydropyrido[4,3-d]pyrimidine-5(6H)-thione (150 mg, 0.4 mmol), (2S,4R)-1-tert-butyl 2-methyl 4-(aminooxy)pyrrolidine-1,2-dicarboxylate (416 mg, 1.6 mmol), Hg(OAc)2 (256 mg, 0.8 mmol) and toluene (2 mL) was heated at 100° C. for 2 h. Cooled to rt, filtered through celite and purified to afford (2S,4R)-1-tert-butyl 2-methyl 4-((Z)—((R)-2-amino-7-(2-bromo-4-fluorophenyl)-4-methyl-7,8-dihydropyrido[4,3-d]pyrimidin-5(6H)-ylidene)aminooxy)pyrrolidine-1,2-dicarboxylate (172 mg, 570%) as off white solid. MS (ES) [M+H] calculated for C25H31BrFN6O5, 593.14. found 593.10.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071766B2
Source datasetuspto-grants-2011_12
ORD IDord-24be41d3ab3a4d25b542befd11cf2141
Source noteuspto-grants-2011_12