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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972086Generated: October 31, 2026

tert-Butyl 3-amino-3-(hydroxymethyl)pyrrolidine-1-carboxylate → HCID 67373624, compound

https://huagongshe.com/reaction/1972086

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 3-amino-3-(hydroxymethyl)pyrrolidine-1-carboxylateHCID 24730317—
Reactant6-Butyl-5-(4-cyclohexyloxy-phenyl)-pyridazine-3-carboxylic acid pentafluorophenyl esterHCID 86657823—
Solvent1,2-DichloroethaneHCID 11—
SolventEthyl AcetateHCID 8857—
ProductHCID 67373624HCID 67373624—

Reaction Steps

To a mixture of 3-amino-3-hydroxymethyl-pyrrolidine-1-carboxylic acid tert-butyl ester (1.0 mmol, 0.21 g) in anhydrous DCE (2 mL), 6-butyl-5-(4-cyclohexyloxy-phenyl)-pyridazine-3-carboxylic acid pentafluorophenyl ester (Example 93, 0.5 mmol, 0.26 g) and TEA (0.5 mL) was stirred at room temperature for 3 h. The reaction mixture was diluted with ethyl acetate (10 mL) and washed with NaOH (0.5 M) solution, water, and brine, dried (Na2SO4), filtered and concentrated under reduced pressure. The residue was purified by flash silica gel column chromatography using ethyl acetate:hexanes (7:3) to provide 3-{[6-butyl-5-(4-cyclohexyloxy-phenyl)-pyridazine-3-carbonyl]-amino}-3-hydroxymethyl-pyrrolidine-1-carboxylic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431575B2
Source datasetuspto-grants-2013_04
ORD IDord-563b03fee26d44aa83361b28f91688df
Source noteuspto-grants-2013_04