tert-butyl{3-[4-(2-fluoroethoxy)-2,6-dimethoxyphenyl]-6-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl}carbamate

Base Information

Chemical Name:tert-butyl{3-[4-(2-fluoroethoxy)-2,6-dimethoxyphenyl]-6-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl}carbamate
CAS No.:1290128-15-2
Molecular Formula:C₂₁H₂₆FN₃O₆S
Molecular Weight:467.518
Hs Code.:

Synonyms:tert-butyl{3-[4-(2-fluoroethoxy)-2,6-dimethoxyphenyl]-6-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl}carbamate

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Chemical Property of tert-butyl{3-[4-(2-fluoroethoxy)-2,6-dimethoxyphenyl]-6-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl}carbamate

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Technology Process of tert-butyl{3-[4-(2-fluoroethoxy)-2,6-dimethoxyphenyl]-6-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl}carbamate

There total 8 articles about tert-butyl{3-[4-(2-fluoroethoxy)-2,6-dimethoxyphenyl]-6-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl}carbamate 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:

: 762-51-6
1-fluoro-2-iodoethane

: 1190854-87-5
tert-butyl[3-(4-hydroxy-2,6-dimethoxyphenyl)-6-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl]carbamate

: 1290128-15-2
tert-butyl{3-[4-(2-fluoroethoxy)-2,6-dimethoxyphenyl]-6-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl}carbamate

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 20.5h;

Reference yield:

: 1190854-61-5
ethyl 6-methoxypyrazolo[5,1-b][1,3]thiazole-7-carboxylate

: 1290128-15-2
tert-butyl{3-[4-(2-fluoroethoxy)-2,6-dimethoxyphenyl]-6-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl}carbamate

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium hydroxide; water / ethanol / 2 h / 20 - 80 °C

1.2: Cooling with ice

1.3: 1.5 h / 60 °C

2.1: hydrogenchloride; sodium nitrite / water / 0.5 h / 20 °C / Cooling with ice

2.2: Cooling with ice

2.3: 5 h / 20 °C / 760.05 Torr

3.1: triethylamine / dichloromethane / 11 h / 20 °C

4.1: n-butyllithium / hexane; tetrahydrofuran / 0.67 h / -78 °C

4.2: 2 h

5.1: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / water / 2.58 h / 110 °C / Reflux

6.1: potassium carbonate / N,N-dimethyl-formamide / 20.5 h / 20 °C

With hydrogenchloride; n-butyllithium; water; potassium carbonate; triethylamine; sodium hydroxide; sodium nitrite; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; ethanol; hexane; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 1190854-65-9
tert-butyl (3-bromo-6-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl)carbamate

: 1290128-15-2
tert-butyl{3-[4-(2-fluoroethoxy)-2,6-dimethoxyphenyl]-6-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl}carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / water / 2.58 h / 110 °C / Reflux

2: potassium carbonate / N,N-dimethyl-formamide / 20.5 h / 20 °C

With potassium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In water; N,N-dimethyl-formamide;