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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095327Generated: October 31, 2026

Sodium borohydride → [4-({[3-(6-Amino-2-butoxy-8-methoxy-9H-purin-9-yl)propyl]amino}methyl)phenyl]acetic acid

https://huagongshe.com/reaction/1095327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-(4-formylphenyl)acetic AcidHCID 11344187—
Reactant9-(3-Aminopropyl)-2-butoxy-8-methoxy-9H-purin-6-amineHCID 23158546—
CatalystMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product[4-({[3-(6-Amino-2-butoxy-8-methoxy-9H-purin-9-yl)propyl]amino}methyl)phenyl]acetic acidHCID 66781394—

Reaction Steps

The product from step (vii) (9.7 g) and (4-formylphenyl)acetic acid (5.4 g) were dissolved in THF (100 ml) and stirred at rt for 4 h. Sodium borohydride (1.9 g) and 5 drops of methanol was added and stirred at a rt overnight. The mixture was quenched with water and concentrated under reduced pressure. Water was added and washed with diethyl ether. 0.1N—HCl was added to acidify the solution to pH 6. The suspension was filtered and the solid collected and dried under reduced pressure to give the subtitle compound. Yield 13 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138172B2
Source datasetuspto-grants-2012_03
ORD IDord-e10b7082a4f24b19882071410c319e22
Source noteuspto-grants-2012_03