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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1617183Generated: October 25, 2026

Methanol → (S)-2-(4-((2-Amino-4-(1-hydroxyheptan-3-ylamino)-6-methylpyrimidin-5-yl)methyl)-3-fluorophenyl)acetic acid

https://huagongshe.com/reaction/1617183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium HydroxideHCID 14797—
Reactant(S)-2-(4-((2-Amino-4-(1-hydroxyheptan-3-ylamino)-6-methylpyrimidin-5-yl)methyl)-3-fluorophenyl)acetonitrileHCID 68954091—
Product(S)-2-(4-((2-Amino-4-(1-hydroxyheptan-3-ylamino)-6-methylpyrimidin-5-yl)methyl)-3-fluorophenyl)acetic acidHCID 68956559—

Reaction Conditions

Temperature70 °C

Reaction Steps

A 5M aqueous solution of potassium hydroxide (0.58 mL) was added to a stirred solution of the product from step (iv) (0.11 g) in MeOH (1.5 mL). The mixture was heated at 70° C. for 15 h. The solvent was evaporated under reduced pressure and the aqueous residue was adjusted to pH ˜7 with concentrated HCl. The aqueous was extracted with EtOAc and the combined organic phase was dried, filtered and evaporated to the subtitle compound, 0.102 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765939B2
Source datasetuspto-grants-2014_07
ORD IDord-b20c91ec4c134d3893fc3df069e25c3f
Source noteuspto-grants-2014_07