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A sdsu.instructure.com Dashboard final group synthesis activity + Please provide a synthesis of the molecule assigned to your team. Each of these molecules are FDA approved drugs that have made it to patients in the last 5 years. You don't need to, but I encourage you to look into what your team's molecule is used for. Some drugs come as a salt. Do not worry about the counterion, just make the drug. No need to worry about chirality or forming any rings from scratch. Each team gets 1 'life-line' if they choose to use it. Simply email Professor Gustafson with the bond you are having trouble forming and he will give you a hint. Team 1: Team 4: God CCHE HN RETEVMO TAZVERIK Team 2: Team 5: HN-CH < jamboard.google.com SOLUTION: final group synthesis activity - Chemistry Homework Help - Studypool Ochem final synthesis: Group 4 - Google Jamboard + Ochem final synthesis: Group 4 3/4 CMS +2 : Share T n ?? Set background Clear frame - Open on a Jamboard Synthesis → -ce H-N Buli Benzyne formation , ? ?? SNAR (A) He altce . ? -H+ form Formyl chloride (B) (0) ·ce H Coxidation) To] Croz convert aldehyde to acid [ O -OH (E) -H (D) morpholine attack G G ? -NH2 HN 2 Chapa Product (F) ( (1) HAN Br Br Br I what STAB ? 43 O Reductive amination methyl 5-bromo-2-methyl- 3-nitrobenzoate ($24gram) CH3CHO, STAB Also another red aminanon are H3co T H?C H3CO HSCO. you coupling this N STAB? Vols reaction diffon with Papphu Na2CO3 → Suzuki 2 NaOH ETOH Hy Tuin ester H3CO HO Bonnie to carb. acid Acid double Chelt this... o 1) DCC Not risht Strupe 2) NHA #3 IN Product! 0 HN ???? •CH3 HN H3C -CH3
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