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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387793Generated: October 26, 2026

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

https://huagongshe.com/reaction/2387793

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-3-aminoheptan-1-olHCID 55290391—
Reactanttert-Butyl 3-(2-amino-4-chloro-6-methylpyrimidin-5-yl)prop-2-ynylcarbamateHCID 86633394—
Solvent1-ButanolHCID 263—
Product(S)-tert-Butyl 3-(2-amino-4-(1-hydroxyheptan-3-ylamino)-6-methylpyrimidin-5-yl)prop-2-ynylcarbamateHCID 8663339564.4%

Reaction Steps

The product from step (vi) (200 mg) and the product from step (v) (177 mg) were combined in butan-1-ol (5 mL) and reacted in a CEM Microwave, at 120° C. for 1 h. The solvents were evaporated, and the crude product was purified by chromatography, eluting with 5% MeOH in EtOAc to afford the subtitle compound 170 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268990B2
Source datasetuspto-grants-2012_09
ORD IDord-3697877e14f74c54a0a642a940226da5
Source noteuspto-grants-2012_09