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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796677Generated: November 4, 2026

Benzyl Alcohol → {3-Cyano-4-[4-(2-methoxy-phenoxy)-phenylamino]-5-methyl-pyrrolo[1,2-b]pyridazin-6-yl}-carbamic acid benzyl ester

https://huagongshe.com/reaction/1796677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant3-Cyano-4-[4-(2-methoxy-phenoxy)-phenylamino]-5-methyl-pyrrolo[1,2-b]pyridazine-6-carboxylic acidHCID 22179667—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product{3-Cyano-4-[4-(2-methoxy-phenoxy)-phenylamino]-5-methyl-pyrrolo[1,2-b]pyridazin-6-yl}-carbamic acid benzyl esterHCID 2079157375.1%

Reaction Steps

A mixture of 430D (1.24 g, 3.0 mmol), Et3N (1.67 ml, 12.0 mmol) and DPPA (1.29 ml, 6.0 mmol) in 1,4-dioxane (20 ml) was stirred at rt for 16 h under argon. Benzyl alcohol (1.86 ml, 18.0 mmol) was added. The resulting mixture was heated to 80° C. for 2.5 h, cooled to rt. Removal of the solvent in vacuo gave a brown oil. Treated with EtOAc (100 ml), the mixture was washed with H2O (3×30 ml) and brine (20 ml), dried with Na2SO4. Removal of the solvent followed by flash chromatography of the residue on silica gel (CH2Cl2 first, then 20% EtOAc-hexanes) gave 430E (1.17 g, 75%) as a light yellow solid. It has a retention time of 6.96 min (standard LC1 method, 8 min run). MS Found: (M+H)+=520.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030112B2
Source datasetuspto-grants-2006_04
ORD IDord-aed8b583dfdf470c9370ed17e993304f
Source noteuspto-grants-2006_04