(S)-2-((4-fluorobenzyl)carbaMoyl)-7-Methoxy-4,10-dioxo-4,6,7,8,9,10-hexahydropyriMido[1,2-a]azepin-3-yl Methanesulfonate

Base Information

Chemical Name:(S)-2-((4-fluorobenzyl)carbaMoyl)-7-Methoxy-4,10-dioxo-4,6,7,8,9,10-hexahydropyriMido[1,2-a]azepin-3-yl Methanesulfonate
CAS No.:1220510-49-5
Molecular Formula:C19H20FN3O7S
Molecular Weight:503.531
Hs Code.:
Mol file:1220510-49-5.mol

Synonyms:(S)-2-((4-fluorobenzyl)carbaMoyl)-7-Methoxy-4,10-dioxo-4,6,7,8,9,10-hexahydropyriMido[1,2-a]azepin-3-yl Methanesulfonate

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Chemical Property of (S)-2-((4-fluorobenzyl)carbaMoyl)-7-Methoxy-4,10-dioxo-4,6,7,8,9,10-hexahydropyriMido[1,2-a]azepin-3-yl Methanesulfonate

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Technology Process of (S)-2-((4-fluorobenzyl)carbaMoyl)-7-Methoxy-4,10-dioxo-4,6,7,8,9,10-hexahydropyriMido[1,2-a]azepin-3-yl Methanesulfonate

There total 1 articles about (S)-2-((4-fluorobenzyl)carbaMoyl)-7-Methoxy-4,10-dioxo-4,6,7,8,9,10-hexahydropyriMido[1,2-a]azepin-3-yl Methanesulfonate 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:

: 1220511-15-8
(7S,10R)-10-[[(dimethylamino)(oxo)acetyl](ethyl)amino]-2-{[(4-fluorobenzyl)amino]carbonyl}-7-methoxy-4-oxo-4,6,7,8,9,10-hexahydropyrimido[1,2-a]azepin-3-yl methanesulfonate

: 1220510-49-5
N-ethyl-N-((7S,10R)-2-{[(4-fluorobenzyl)amino]carbonyl}-3-hydroxy-7-methoxy-4-oxo-4,6,7,8,9,10-hexahydropyrimido[1,2-a]azepin-10-yl)-N,N-dimethylethanediamide

Guidance literature:: (7S,10R)-10-[[(dimethylamino)(oxo)acetyl](ethyl)amino]-2-{[(4-fluorobenzyl)amino]carbonyl}-7-methoxy-4-oxo-4,6,7,8,9,10-hexahydropyrimido[1,2-a]azepin-3-yl methanesulfonate; With isopropyl alcohol; sodium hydroxide; at 20 - 25 ℃; for 0.5h;

With hydrogenchloride; In isopropyl alcohol;