反应详情
EQUATION
反应方程式
REACTANTS
反应物
Ethylenediaminetetraacetic acid
C10H16N2O8
Benzoic acid, 3,3'-dithiobis[6-nitro-
C14H8N2O8S2
Acetic anhydride
C4H6O3
1H-Indole-3-ethanol
C10H11NO
Trisodium phosphate
Na3O4P
Tryptamine hydrochloride
C10H13ClN2
2 次
9-{5-O-[{[(4-{[3-(Ethylimino)-3-hydroxypropyl]imino}-3,4-dihydroxy-2,2-dimethylbutoxy)(hydroxy)phosphoryl]oxy}(hydroxy)phosphoryl]-3-O-phosphonopentofuranosyl}-9H-purin-6-amine
C21H36N7O16P3
Acetyl CoA
C23H38N7O17P3S
Dithiothreitol
C4H10O2S2
未命名化合物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
The following were purchased: acetyl-CoA (Pharmacia Biotech Inc.); tryptamine-HCl, desulfo-CoA, glutathione-agarose, DTNB (Sigma); sodium phosphate, dithiothreitol, guanidinium-HCl, EDTA (Fisher Scientific); tryptophol (Aldrich); and [14C]acetyl-CoA (60 Ci/mol) (NEN Life Science Products). N-acetyltryptamine was synthesized by reacting tryptamine-HCl (500 mg, 2.5 mmol) with acetic anhydride (260 mg, 2.5 mmol) in the presence of excess triethylamine (1.75 ml). After vigorous stirring at room temperature for 50 min, the mixture was partitioned between ethyl acetate (80 ml) and water (70 ml). The organic phase was washed with saturated aqueous NaHCO3 (50 ml), 0.1 M HCl (50 ml), Na2SO4 (anhydride), and the resultant was concentrated in vacuo to afford N-acetyltryptamine as off-white crystals (88% yield). Purity (>95%) was established by TLC and 1H NMR.
WORKUP
后处理
- customN-acetyltryptamine was synthesized
- customthe mixture was partitioned between ethyl acetate (80 ml) and water (70 ml)
- washThe organic phase was washed with saturated aqueous NaHCO3 (50 ml), 0.1 M HCl (50 ml), Na2SO4 (anhydride)
- concentrationthe resultant was concentrated in vacuo