2-[3-(4',5'-difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-benzyl]-1,1-dioxo-1λ6-[1,2]thiazinane-3-carboxylic acid tert-butyl ester

Base Information

Chemical Name:2-[3-(4',5'-difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-benzyl]-1,1-dioxo-1λ6-[1,2]thiazinane-3-carboxylic acid tert-butyl ester
CAS No.:1310039-00-9
Molecular Formula:C₃₀H₃₃F₂NO₆S
Molecular Weight:573.658
Hs Code.:

Synonyms:2-[3-(4',5'-difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-benzyl]-1,1-dioxo-1λ6-[1,2]thiazinane-3-carboxylic acid tert-butyl ester

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Chemical Property of 2-[3-(4',5'-difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-benzyl]-1,1-dioxo-1λ6-[1,2]thiazinane-3-carboxylic acid tert-butyl ester

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Technology Process of 2-[3-(4',5'-difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-benzyl]-1,1-dioxo-1λ6-[1,2]thiazinane-3-carboxylic acid tert-butyl ester

There total 11 articles about 2-[3-(4',5'-difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-benzyl]-1,1-dioxo-1λ6-[1,2]thiazinane-3-carboxylic acid tert-butyl ester 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:

: 82072-23-9
3-(bromomethyl)benzaldehyde

: 1310039-00-9
2-[3-(4',5'-difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-benzyl]-1,1-dioxo-1λ6-[1,2]thiazinane-3-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / acetone / Reflux

2.1: lithium aluminium tetrahydride / tetrahydrofuran / 1 h / 20 °C / Cooling with ice

2.2: 0.08 h

3.1: phosphorus tribromide / dichloromethane / 6 h / 0 - 20 °C

4.1: potassium carbonate / N,N-dimethyl-formamide / 20 °C

With lithium aluminium tetrahydride; phosphorus tribromide; potassium carbonate; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; acetone;

Reference yield:

: 1310036-86-2
4'-(3-bromomethyl-benzyloxy)-4,5-difluoro-2-methoxy-biphenyl

: 1310037-39-8
1,1-dioxo-1λ6-[1,2]thiazinane-3-carboxylic acid tert-butyl ester

: 1310039-00-9
2-[3-(4',5'-difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-benzyl]-1,1-dioxo-1λ6-[1,2]thiazinane-3-carboxylic acid tert-butyl ester

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃;

Reference yield:

: 117997-81-6
5-(benzyloxy)-2-(tert-butoxycarbonylamino)-5-oxopentanoic acid

: 1310039-00-9
2-[3-(4',5'-difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-benzyl]-1,1-dioxo-1λ6-[1,2]thiazinane-3-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 7 steps

1.1: dicyclohexyl-carbodiimide / dmap / dichloromethane / 1 h / 20 °C

2.1: hydrogen / palladium on activated charcoal / ethanol / 2 h / 2327.23 Torr

3.1: 4-methyl-morpholine; isobutyl chloroformate / tetrahydrofuran / -20 °C

3.2: 2 h / Cooling with ice

4.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 0.5 h

4.2: 5 h / 20 °C / Cooling with ice

5.1: sodium acetate; acetic acid / water / 0.17 h / Cooling with ice

6.1: trifluoroacetic acid / dichloromethane / 2 h / 20 °C / Cooling with ice

7.1: potassium carbonate / N,N-dimethyl-formamide / 20 °C

With 4-methyl-morpholine; di-isopropyl azodicarboxylate; hydrogen; sodium acetate; potassium carbonate; acetic acid; dicyclohexyl-carbodiimide; triphenylphosphine; trifluoroacetic acid; isobutyl chloroformate; dmap; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; water; N,N-dimethyl-formamide;