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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154690Generated: October 25, 2026

Acetic Acid → 4-(N-((2,4-diamino-6-pteridinyl)methyl)amino)benzoic acid

https://huagongshe.com/reaction/1154690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium HydroxideHCID 14798—
ReactantAminopterinHCID 169371—
CatalystZincchlorideHCID 3007855—
SolventSodium AcetateHCID 517045—
Product4-(N-((2,4-diamino-6-pteridinyl)methyl)amino)benzoic acidHCID 16974886%

Reaction Conditions

Temperature5 °C

Reaction Steps

Aminopterin (2.4 g, 0.005 mol) is suspended in 1M NaOAc (500 ml) containing ZnCl2 (0.1 g), and 2N NaOH is added dropwise with stirring until a clear solution forms. Glacial AcOH is then added dropwise to bring the pH to 7.5, and 5 μl of carboxypeptidase G1 (4000 units/ml) is added. The mixture is shaken at 37° C. for 1 day, cooled to 5° C., and suction filtered. The solid is washed thoroughly with H2O, and dried in vacuo on a freeze-drying apparatus to obtain 4-amino-4-deoxypteroic acid (APA) (1.43 g, 86%) as an orange-yellow solid. The analytical sample is prepared by passing a small amount of this material through a microcrystalline cellulose column, with 0.1M glycine, pH 10, as the eluent. Appropriate fractions are pooled and acidified with AcOH, and the precipitate is collected, washed with H2O, and dried in vacuo over P2O5 ; Rf 0.1 (cellulose, pH 7.4 phosphate), dark absorbing spot; UVλmax (0.1N HCl) 243 nm (ε 18,500), 297 (23,900), 337 infl (13,700); UVλmax (0.1N NaOH) 261 nm (ε 30,400), 371 (9,100). Analysis for C, H, and N confirms the composition of APA.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04490529
Source datasetuspto-grants-1984_12
ORD IDord-26775886c76d4b87810420f33ba47ed3
Source noteuspto-grants-1984_12