ethyl 3-{[(benzyloxy)carbonyl]amino}-7-bromoquinoline-2-carboxylate

Base Information

• Chemical Name: ethyl 3-{[(benzyloxy)carbonyl]amino}-7-bromoquinoline-2-carboxylate
• CAS No.: 1620239-11-3
• Molecular Formula: C₂₀H₁₇BrN₂O₄
• Molecular Weight: 429.27
• Mol file: 1620239-11-3.mol

Synonyms:ethyl 3-{[(benzyloxy)carbonyl]amino}-7-bromoquinoline-2-carboxylate

Chemical Property of ethyl 3-{[(benzyloxy)carbonyl]amino}-7-bromoquinoline-2-carboxylate

Chemical Property:

Purity/Quality:

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Technology Process of ethyl 3-{[(benzyloxy)carbonyl]amino}-7-bromoquinoline-2-carboxylate

There total 1 articles about ethyl 3-{[(benzyloxy)carbonyl]amino}-7-bromoquinoline-2-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

ethyl 3-amino-7-bromoquinoline-2-carboxylate (1260807-99-5) + benzyl chloroformate (501-53-1,94274-21-2) → ethyl 3-{[(benzyloxy)carbonyl]amino}-7-bromoquinoline-2-carboxylate (1620239-11-3)

Guidance literature:

With pyridine; In dichloromethane; at -10 - 20 ℃; for 1h;

Reference yield: 76.0%

ethyl 3-{[(benzyloxy)carbonyl]amino}-7-bromoquinoline-2-carboxylate (1620239-11-3) → 3-{[(benzyloxy)carbonyl]amino}-7-bromoquinoline-2-carboxylic acid (1620239-12-4)

Guidance literature:

With potassium phosphate; In 1,4-dioxane; water; at 100 ℃; for 3h;

Reference yield: 60.0%

ethyl 3-{[(benzyloxy)carbonyl]amino}-7-bromoquinoline-2-carboxylate (1620239-11-3) + 2,6-difluorophenylboronic acid (162101-25-9) → ethyl 3-(((benzyloxy)carbonyl)amino)-7-(2,6-difluorophenyl)quinoline-2-carboxylate

Guidance literature:

With chloro(2-dicyclohexylphosphino-2’,4’,6’-triisopropyl-1,1‘-biphenyl)[2-(2’-amino-1,1‘-biphenyl’)]palladium(II); In 1,4-dioxane; water; at 60 ℃; for 2h; Inert atmosphere;

upstream raw materials:

ethyl 3-amino-7-bromoquinoline-2-carboxylate

benzyl chloroformate

Downstream raw materials:

ethyl 3-{[(benzyloxy)carbonyl]amino}-7-morpholin-4-ylquinoline-2-carboxylate

3-{[(benzyloxy)carbonyl]amino}-7-vinylquinoline-2-carboxylic acid

benzyl (2-{[(4-{(3S)-3-[(tert-butoxycarbonyl)amino]piperidin-1-yl}pyridin-3-yl)amino]carbonyl}-7-vinylquinolin-3-yl)carbamate

benzyl (2-{[(4-{(3S)-3-[(tert-butoxycarbonyl)amino]piperidin-1-yl}pyridin-3-yl)amino]carbonyl}-7-formylquinolin-3-yl)carbamate