돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1154690생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1154690

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium HydroxideHCID 14798—
반응물AminopterinHCID 169371—
촉매ZincchlorideHCID 3007855—
용매Sodium AcetateHCID 517045—
생성물4-(N-((2,4-diamino-6-pteridinyl)methyl)amino)benzoic acidHCID 16974886%

반응 조건

온도5 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04490529
출처 데이터셋uspto-grants-1984_12
ORD IDord-26775886c76d4b87810420f33ba47ed3
출처 메모uspto-grants-1984_12