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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386567Generated: October 25, 2026

Isobutane → tert-Butyl 4-(3-carbamoyl-1-(4-cyano-3-fluorophenyl)-6-oxo-1,6-dihydropyridazin-4-yloxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/386567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutaneHCID 6360—
ReactantMethyl 4-(1-(tert-butoxycarbonyl)piperidin-4-yloxy)-1-(4-cyano-3-fluorophenyl)-6-oxo-1,6-dihydropyridazine-3-carboxylateHCID 44620996—
Reactant1-(4-(Methylsulfonyl)phenyl)-6-oxo-1,6-dihydropyridazine-3-carboxylateHCID 86658658—
Producttert-Butyl 4-(3-carbamoyl-1-(4-cyano-3-fluorophenyl)-6-oxo-1,6-dihydropyridazin-4-yloxy)piperidine-1-carboxylateHCID 6744541691%

Reaction Steps

tert-Butyl 4-(3-carbamoyl-1-(4-cyano-3-fluorophenyl)-6-oxo-1,6-dihydropyridazin-4-yloxy)piperidine-1-carboxylate was prepared in 91% yield according to procedures described in Example 31 (Step A) substituting methyl 441-(tert-butoxycarbonyl)piperidin-4-yloxy)-1-(4-(methylsulfonyl)phenyl)-6-oxo-1,6-dihydropyridazine-3-carboxylate for methyl 4-(1-(tert-butoxycarbonyl)piperidin-4-yloxy)-1-(4-cyano-3-fluorophenyl)-6-oxo-1,6-dihydropyridazine-3-carboxylate (example 29). MS (ESI) 402 (M+H-tBu).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372837B2
Source datasetuspto-grants-2013_02
ORD IDord-b3d7758759f2471b81a8c11237c59839
Source noteuspto-grants-2013_02