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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264584Generated: October 30, 2026

HCID 59596400, compound → HCID 59596404, compound

https://huagongshe.com/reaction/2264584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59596400HCID 59596400—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 59596404HCID 59596404—

Reaction Steps

250 mg (0.42 mMol) of 7-(2-amino-6-chloro-pyrimidin-4-yloxy)-2,3,4,5-tetrahydro-benzo[b]azepine-1-carboxylic acid [3-trifluoromethyl-4-(4-methylpiperazin-1-ylmethyl)-phenyl]-amide in 35 ml methanol are hydrogenated in the presence of 160 mg Pd/C (10%; Engelhard 4505). The catalyst is filtered off, the filtrate diluted with EtOAc and sat. Na2CO3/H2O 1:1 and the separated aqueous layer extracted twice with water. The organic layers are washed with water and brine, dried (Na2SO4) and concentrated. Reversed phase MPLC (Gilson system) gives the title compound: MS: [M+1]+=556; HPLC: AtRet=9.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855215B2
Source datasetuspto-grants-2010_12
ORD IDord-b8c7a00f185c4cd382a0e639176eada3
Source noteuspto-grants-2010_12