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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216524Generated: October 27, 2026

2-[(E)-[1-(2-aminothiazol-4-yl)-2-oxo-2-(2-oxoethylamino)ethylidene]amino]oxy-2-methyl-propanoic acid → 5-[4-(Benzyloxy)phenyl]-4-bromo-1-cyclohexyl-1h-pyrazole-3-carbaldehyde

https://huagongshe.com/reaction/2216524

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[(E)-[1-(2-aminothiazol-4-yl)-2-oxo-2-(2-oxoethylamino)ethylidene]amino]oxy-2-methyl-propanoic acidHCID 15956689—
Reactant{5-[4-(Benzyloxy)phenyl]-4-bromo-1-cyclohexyl-1h-pyrazol-3-yl}methanolHCID 21943365—
Product5-[4-(Benzyloxy)phenyl]-4-bromo-1-cyclohexyl-1h-pyrazole-3-carbaldehydeHCID 2194332182.5%

Reaction Steps

Aldehyde 8.3 was prepared from 8.2 according to the procedure described above for the preparation aldehyde 2.2. In this example, 8.2 (295 mg, 0.668 mmol) was oxidized to yield 242 mg (82%) of 8.3. MS (ESI) 439.3 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112601B2
Source datasetuspto-grants-2006_09
ORD IDord-db3ae2023c2c4db186a0d90684d589c5
Source noteuspto-grants-2006_09