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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755404Generated: October 31, 2026

1-Methylimidazole → Tert-butyl 4-(1-(8-(5,6-dimethoxypyridin-2-ylamino)imidazo[1,2-b]pyridazin-6-yl)pyrrolidine-3-carboxamido)benzoate

https://huagongshe.com/reaction/1755404

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylimidazoleHCID 1390—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantBenzoic acid, 4-amino-, 1,1-dimethylethyl esterHCID 233272—
Reactant1-(8-(5,6-Dimethoxypyridin-2-ylamino)imidazo[1,2-b]pyridazin-6-yl)pyrrolidine-3-carboxylic acidHCID 86682746—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(1-(8-(5,6-dimethoxypyridin-2-ylamino)imidazo[1,2-b]pyridazin-6-yl)pyrrolidine-3-carboxamido)benzoateHCID 86682747170.2%

Reaction Steps

A mixture of 1-(8-(5,6-dimethoxypyridin-2-ylamino)imidazo[1,2-b]pyridazin-6-yl)pyrrolidine-3-carboxylic acid (80 mg, 0.21 mmol), tert-butyl 4-aminobenzoate (40 mg, 0.21 mmol), EDCI (159 mg, 0.08 mmol) and 1-methyl-1H-imidazole (68 mg, 0.8 mmol) in dichloromethane (5 mL) was stirred at room temperature for 16 h. The residue was concentrated to give crude tert-butyl 4-(1-(8-(5,6-dimethoxypyridin-2-ylamino)imidazo[1,2-b]pyridazin-6-yl)pyrrolidine-3-carboxamido)benzoate (200 mg, crude) as brown liquid that was used directly without purification. LC-MS: 560 [M+1]+, tR=1.510 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169259B2
Source datasetuspto-grants-2015_10
ORD IDord-20e50a74b0bb4f2e8ae5d92605401101
Source noteuspto-grants-2015_10