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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877731Generated: November 3, 2026

Potassium Phosphate, Tribasic → (R)-tert-butyl 4-(3-carbamoyl-6-(6-methoxypyridin-3-yl)pyrrolo[1,2-b]pyridazin-4-ylamino)-3,3-dimethylpiperidine-1-carboxylate

https://huagongshe.com/reaction/877731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant(6-Methoxypyridin-3-yl)boronic acidHCID 2734368—
Reactant(R)-tert-butyl 4-(6-bromo-3-carbamoylpyrrolo[1,2-b]pyridazin-4-ylamino)-3,3-dimethylpiperidine-1-carboxylateHCID 68291074—
Catalystpalladium(II) acetateHCID 167845—
CatalystBis(ditert-butyl(cyclopenta-2,4-dien-1-yl)phosphane);iron(2+)HCID 12976736—
SolventDimethylformamideHCID 6228—
Product(R)-tert-butyl 4-(3-carbamoyl-6-(6-methoxypyridin-3-yl)pyrrolo[1,2-b]pyridazin-4-ylamino)-3,3-dimethylpiperidine-1-carboxylateHCID 68292118102.3%

Reaction Conditions

Temperature90 °C

Reaction Steps

A stirred DMF (8.0 mL) solution of (R)-tert-butyl 4-(6-bromo-3-carbamoylpyrrolo[1,2-b]pyridazin-4-ylamino)-3,3-dimethylpiperidine-1-carboxylate (1.20 g, 2.57 mmol), 6-methoxypyridin-3-ylboronic acid (0.787 g, 5.15 mmol), potassium phosphate (1.639 g, 7.72 mmol), palladium acetate (0.058 g, 0.257 mmol) and 1,1′-Bis(di-tert-butylphosphino)ferrocene (0.124 g, 0.257 mmol) was degassed by purging with argon for 5 min. The sealed tube was then heated at 90° C. for 1 h then cooled and partitioned between ethyl acetate and water. The layers were separated and the organic portion was washed with water, 10% LiCl (×2), brine and dried over anhyd. magnesium sulfate, filtered and concentrated under vacuum to afford the title compound as a tan solid (1.30 g, quantitative). HPLC (Method B) retention time=3.90 min. LCMS (m+1)=495.3. Material contained ˜10% of unreacted bromide starting material but was used without any further purification in next transformation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987268B2
Source datasetuspto-grants-2015_03
ORD IDord-d1e41994a9334d61aabcec02ab754d7c
Source noteuspto-grants-2015_03