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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507507Generated: November 2, 2026

HCID 136504501, compound → HCID 136504489, compound

https://huagongshe.com/reaction/1507507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 136504501HCID 136504501—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductHCID 136504489HCID 13650448994%

Reaction Steps

Into a 10-mL round-bottom flask purged and maintained with an atmosphere of hydrogen, was placed a solution of benzyl 4-[5-(1,3-benzothiazol-2-yl)-4-[[(3R)-1-[(tert-butoxy)carbonyl]piperidin-3-yl]amino]-6-oxo-1,6-dihydropyrimidin-2-yl]piperidine-1-carboxylate (644 mg, 1.00 mmol, 1.00 equiv), Palladium carbon (64.4 mg) and methanol (20 mL). The resulting mixture was stirred overnight at room temperature. Filtration and evaporation gave 480 mg (94%) of the title compound as a light yellow solid, which was used directly for next step without further purification. MS m/z [M+H]+ (ESI): 511.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221809B2
Source datasetuspto-grants-2015_12
ORD IDord-c839d8c0c9f2442b8a0a494954e18719
Source noteuspto-grants-2015_12