A kind of synthesis method of synthetic marijuana antigen and the application of synthetic marijuana antigen
A technology for synthesizing hemp and synthetic methods, which is applied in the field of immunoassays, can solve the problems of large space occupation, high price, unfavorable industrial production, etc., and achieve the effects of easy portability, long-term storage, and stability
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0025] The preparation of 1.3-(1-naphthoyl) indole: under the protection of nitrogen, in the round bottom flask, the naphthoyl chloride of 754.8mg is dissolved in 16ml of anhydrous dichloromethane, then add the anhydrous aluminum chloride of 717mg , stirred for 20min, the solution was yellow-green. Dissolve 351.45mg of indole in 6ml of anhydrous dichloromethane, then drop it into a round bottom flask, and continue stirring for 3h. The progress of the reaction was detected by TLC, and the developer petroleum ether: ethyl acetate = 4:1. After the reaction, the solution turns yellow; put the reaction system in an ice-water bath, then slowly add 45ml of ice water, transfer to a separatory funnel to separate the organic phase; extract with 2*45ml of dichloromethane, combine the organic phases, and wash with saturated saline , evaporated to dryness under reduced pressure, and obtained 606mg of 3-(1-naphthoyl)indole by column chromatography, yield 74.54%. The structure of the obtai...
Embodiment 2
[0052] The difference with Example 2 is that: during the preparation of 2-(3-(1-naphthoyl)indole-1-)ethyl acetate, ethyl bromoacetate is replaced with propyl bromoacetate.
Embodiment 3
[0054] A synthetic method for synthesizing cannabis antigens, comprising the following steps,
[0055] A. Take 90mg of (S)-2-(3-(1-naphthoyl)indole-1-)-N-(2-oxytetrahydrothiophene-3-)acetamide prepared in Example 1 and dissolve in 3mL methanol, then add 0.9mL 1N NaOH aqueous solution, after stirring at room temperature for 8min, add 0.9mL 1M hydrochloric acid to obtain (S)-2-(2-(3-(1-naphthylmethyl)indole-1- )acetamide)-4-mercaptobutanoic acid;
[0056] The structure of (S)-2-(2-(3-(1-naphthylmethyl)indole-1-)acetamide)-4-mercaptobutanoic acid is shown in formula (Ⅵ):
[0057]
[0058] B. SPDP is dissolved in DMF, obtains SPDP-DMF solution, and the concentration that makes SPDP in DMF is 28mg / mL;
[0059] Add 0.18mL SPDP-DMF solution dropwise into 1mL BSA solution, react at room temperature for 1h, remove unreacted SPDP, and obtain SPDP-BSA protein solution;
[0060] C. Take 42mL of the SPDP‐BSA protein solution prepared in step B, and drop into (S)‐2‐(2‐(3‐(1‐naphthylme...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


