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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843282Generated: November 2, 2026

Sarcosine → 2-Bromo-6-{4,4-dimethyl-9-oxo-7-thia-10,11-diazatricyclo[6.4.0.02,6]dodeca-1(8),2(6),11-trien-10-yl}-4-fluorobenzaldehyde

https://huagongshe.com/reaction/1843282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSarcosineHCID 1088—
ReactantPotassium CarbonateHCID 11430—
Reactant2,6-Dibromo-4-fluorobenzaldehydeHCID 44474666—
Reactant7,7-Dimethyl-7,8-dihydro-3H-cyclopenta[4,5]thieno[2,3-d]pyridazin-4(6H)-oneHCID 86683783—
Solvent1,4-DioxaneHCID 31275—
Product2-Bromo-6-{4,4-dimethyl-9-oxo-7-thia-10,11-diazatricyclo[6.4.0.02,6]dodeca-1(8),2(6),11-trien-10-yl}-4-fluorobenzaldehydeHCID 86683782—

Reaction Conditions

Temperature95 °C

Reaction Steps

A 100-mL round bottom flask equipped with a magnetic stirrer and a reflux condenser was charged with 131h (330 mg, 1.5 mmol), 2,6-dibromo-4-fluorobenzaldehyde (1.26 g, 4.5 mmol), CuBr (113 mg, 0.8 mmol), sarcosine (142 mg, 1.6 mmol), K2CO3 (420 mg, 3.0 mmol), and dioxane (20 mL). See FIG. 15. After three cycles of vacuum/argon flush, the mixture was heated at 95° C. for 15 h. It was then cooled to room temperature and filtered. The filtrate was concentrated under reduced pressure and the resulting residue was purified by silica-gel column chromatography 5:1 eluting with petroleum ether/ethyl acetate to 131i as a white solid (380 mg, 60%). MS-ESI: [M+H]+ 420.6

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946213B2
Source datasetuspto-grants-2015_02
ORD IDord-69c25d2d2dc74613a2451922174c27cc
Source noteuspto-grants-2015_02