Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862433Generated: October 26, 2026

5-amino-1-methyl-2,3-dihydro-1H-pyrazol-3-one → 4-(4-bromo-3-chlorophenyl)-1-methyl-1,2,4,9-tetrahydropyrano[3,4-b]pyrazolo[4,3-e]pyridine-3,5(6H,8H)-dione

https://huagongshe.com/reaction/1862433

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-amino-1-methyl-2,3-dihydro-1H-pyrazol-3-oneHCID 252198—
Reactant2H-pyran-3,5(4H,6H)-dioneHCID 325287—
Reactant4-Bromo-3-chlorobenzaldehydeHCID 14049806—
Product4-(4-bromo-3-chlorophenyl)-1-methyl-1,2,4,9-tetrahydropyrano[3,4-b]pyrazolo[4,3-e]pyridine-3,5(6H,8H)-dioneHCID 1027301070.7%

Reaction Steps

2H-Pyran-3,5(4H,6H)-dione (0.057 g, 05 mmol), 3-chloro4-bromo-benzaldehyde (0.11 g, 0.5 mmol), and 5-amino-1-methyl-1,2-dihydropyrazol-3-one (0.056g, 0.5 mmol) were processed as described in Example 26C to provide 0.145 g of the title compound. 1H NMR (300 MHz, DMSO-d6) δ 3.5 (s, 3H), 4.0 (s, 2H), 4.52 (q, 2H), 4.92 (s, 1H), 7.03 (dt, 1H), 7.32(t, 1H), 7.6 (dd, 1H), 9.62 (s, 1H), 10.1 (s, 1H); MS (ESI−) m/z 410 (M−H:) Anal. calcd for C16H13N3BrClO3: C, 46.80;H,3.19; N, 10.23. Found: C, 46.77;H, 3.43; N, 10.27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06538004B2
Source datasetuspto-grants-2003_03
ORD IDord-d80d745392fc4a5d8731cd3497ecb475
Source noteuspto-grants-2003_03