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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1617141Generated: November 1, 2026

(S)-tert-Butyl 3-(2-amino-4-(1-hydroxyheptan-3-ylamino)-6-methylpyrimidin-5-yl)prop-2-ynylcarbamate → (S)-tert-Butyl 3-(2-amino-4-(1-hydroxyheptan-3-ylamino)-6-methylpyrimidin-5-yl)propylcarbamate

https://huagongshe.com/reaction/1617141

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-tert-Butyl 3-(2-amino-4-(1-hydroxyheptan-3-ylamino)-6-methylpyrimidin-5-yl)prop-2-ynylcarbamateHCID 86633395—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product(S)-tert-Butyl 3-(2-amino-4-(1-hydroxyheptan-3-ylamino)-6-methylpyrimidin-5-yl)propylcarbamateHCID 8663339675.2%

Reaction Steps

The product from step (vii) (100 mg) and Pd/C (30 mg) in EtOH (5 mL) were hydrogenated under 3 bar at rt for 16 h. The catalyst was filtered off and the solvent evaporated to give the subtitle compound 76 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765939B2
Source datasetuspto-grants-2014_07
ORD IDord-e9ada8e45a29462e8b5b9c5cbeb8da59
Source noteuspto-grants-2014_07