[3-(4-Bromo-2-fluoro-benzyl)-6-chloro-2,4-dioxo-3,4-dihydro-2H-thieno[3,2-d]pyrimidin-1-yl]-acetic acid ethyl ester

Base Information

• Chemical Name: [3-(4-Bromo-2-fluoro-benzyl)-6-chloro-2,4-dioxo-3,4-dihydro-2H-thieno[3,2-d]pyrimidin-1-yl]-acetic acid ethyl ester
• CAS No.: 158460-93-6
• Molecular Formula: C₁₇H₁₃BrClFN₂O₄S
• Molecular Weight: 475.723
• Mol file: 158460-93-6.mol

Synonyms:[3-(4-Bromo-2-fluoro-benzyl)-6-chloro-2,4-dioxo-3,4-dihydro-2H-thieno[3,2-d]pyrimidin-1-yl]-acetic acid ethyl ester

Chemical Property of [3-(4-Bromo-2-fluoro-benzyl)-6-chloro-2,4-dioxo-3,4-dihydro-2H-thieno[3,2-d]pyrimidin-1-yl]-acetic acid ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of [3-(4-Bromo-2-fluoro-benzyl)-6-chloro-2,4-dioxo-3,4-dihydro-2H-thieno[3,2-d]pyrimidin-1-yl]-acetic acid ethyl ester

There total 5 articles about [3-(4-Bromo-2-fluoro-benzyl)-6-chloro-2,4-dioxo-3,4-dihydro-2H-thieno[3,2-d]pyrimidin-1-yl]-acetic acid ethyl 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: 39.0%

[3-(4-Bromo-2-fluoro-benzyl)-2,4-dioxo-3,4-dihydro-2H-thieno[3,2-d]pyrimidin-1-yl]-acetic acid ethyl ester (158460-92-5) → [3-(4-Bromo-2-fluoro-benzyl)-6-chloro-2,4-dioxo-3,4-dihydro-2H-thieno[3,2-d]pyrimidin-1-yl]-acetic acid ethyl ester (158460-93-6)

Guidance literature:

With sulfuryl dichloride; In dichloromethane; at 60 ℃; for 4h;

DOI:10.1016/0223-5234(93)90112-R

Reference yield:

3-aminothiophene-2-carboxylic acid (55341-87-2) → [3-(4-Bromo-2-fluoro-benzyl)-6-chloro-2,4-dioxo-3,4-dihydro-2H-thieno[3,2-d]pyrimidin-1-yl]-acetic acid ethyl ester (158460-93-6)

Guidance literature:

Multi-step reaction with 5 steps

1: 90 percent / CCl₄; dioxane / 4 h / Heating

2: 1.) NaH, 3.) 28percent aq. ammonia

3: 80 percent / 1.5 h / 120 - 130 °C

4: 1.) NaH / 1.) DMF, RT, 1 h, 2.) DMF, RT, 16 h

5: 39 percent / sulfuryl chloride / CH₂Cl₂ / 4 h / 60 °C

With ammonium hydroxide; sulfuryl dichloride; sodium hydride; In 1,4-dioxane; tetrachloromethane; dichloromethane;

DOI:10.1016/0223-5234(93)90112-R

Reference yield:

2H-thieno[3,2-d][1,3]oxazine-2,4(1H)-dione (78756-28-2) → [3-(4-Bromo-2-fluoro-benzyl)-6-chloro-2,4-dioxo-3,4-dihydro-2H-thieno[3,2-d]pyrimidin-1-yl]-acetic acid ethyl ester (158460-93-6)

Guidance literature:

Multi-step reaction with 4 steps

1: 1.) NaH, 3.) 28percent aq. ammonia

2: 80 percent / 1.5 h / 120 - 130 °C

3: 1.) NaH / 1.) DMF, RT, 1 h, 2.) DMF, RT, 16 h

4: 39 percent / sulfuryl chloride / CH₂Cl₂ / 4 h / 60 °C

With ammonium hydroxide; sulfuryl dichloride; sodium hydride; In dichloromethane;

DOI:10.1016/0223-5234(93)90112-R

upstream raw materials:

[3-(4-Bromo-2-fluoro-benzyl)-2,4-dioxo-3,4-dihydro-2H-thieno[3,2-d]pyrimidin-1-yl]-acetic acid ethyl ester

3-aminothiophene-2-carboxylic acid

2H-thieno[3,2-d][1,3]oxazine-2,4(1H)-dione

(2-Carbamoyl-thiophen-3-ylamino)-acetic acid ethyl ester