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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858072Generated: October 31, 2026

HCID 10326621, compound → HCID 10416025, compound

https://huagongshe.com/reaction/858072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10326621HCID 10326621—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 10416025HCID 1041602537%

Reaction Steps

A solution of 5-chloro-1,3-dimethyl-1H-pyrazole-4-sulfonic acid {4-[3-cyclopropylmethyl-1-(2-fluoro-benzyl)-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-8-ylmethyl]-phenyl}-methyl-amide (prepared as described in Example 18, 20 mg, 0.032 mmol) in methanol (20 mL) at 25° C. was treated with 10% Pd/C (100 mg). The reaction mixture was submitted to hydrogenation conditions in a Parr bomb at 48 psi for 2 d. At this time, the reaction mixture was filtered through a pad of celite and washed with 90/10 methylene chloride/methanol solution (75 mL). The filtrated was concentrated in vacuo. The resulting residue was purified by HPLC (20–60% acetonitrile/water) to afford 1,3-dimethyl-1H-pyrazole-4-sulfonic acid {4-[3-cyclopropylmethyl-1-(2-fluoro-benzyl)-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-8-ylmethyl]-phenyl}-methyl-amide (7.0 mg, 37%) as white solid; (ES)+-HRMS m/e calculated for C29H30FN7O4S (M+Na)+ 614.1956, found 614.1955.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148229B2
Source datasetuspto-grants-2006_12
ORD IDord-63155094aa344762abf69cd72b449188
Source noteuspto-grants-2006_12