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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168808Generated: October 30, 2026

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

https://huagongshe.com/reaction/2168808

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 numberUS09045461B2
Source datasetuspto-grants-2015_06
ORD IDord-5893f4c2094b443d8e078c518bddbf75
Source noteuspto-grants-2015_06