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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850273Generated: October 30, 2026

HCID 137328646, compound → HCID 137328645, compound

https://huagongshe.com/reaction/1850273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 137328646HCID 137328646—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 137328645HCID 13732864592.9%

Reaction Steps

To a solution of 3-{4-[4-(tert-butyl-dimethyl-silanyloxymethyl)-piperidin-1-yl]-6-chloro-pyridazin-3-yl}-azetidine-1-carboxylic acid tert-butyl ester (62) (843 mg, 1.7 mmol) in MeOH was added Pd/C (10%, 0.5 g) under nitrogen. The reaction was stirred under hydrogen at RT for 6 h, filtered to remove Pd/C and concentrated to dryness to give 3-{4-[4-(tert-butyl-dimethyl-silanyloxymethyl)-piperidin-1-yl]-pyridazin-3-yl}-azetidine-1-carboxylic acid tert-butyl ester (63) (730 mg, 1.58 mmol yield 92.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957073B2
Source datasetuspto-grants-2015_02
ORD IDord-9d650699fa7343d5847160c8f048fef2
Source noteuspto-grants-2015_02