tert-butyl-2-[2-(4-oxo-4-benzo[d][1,2,3]triazin-3-ylethyl)]-3-(4-thien-3-yl-phenylthio) propionate

Base Information

Chemical Name:tert-butyl-2-[2-(4-oxo-4-benzo[d][1,2,3]triazin-3-ylethyl)]-3-(4-thien-3-yl-phenylthio) propionate
CAS No.:427895-09-8
Molecular Formula:C₂₆H₂₇N₃O₃S₂
Molecular Weight:493.651
Hs Code.:

Synonyms:tert-butyl-2-[2-(4-oxo-4-benzo[d][1,2,3]triazin-3-ylethyl)]-3-(4-thien-3-yl-phenylthio) propionate

Suppliers and Price of tert-butyl-2-[2-(4-oxo-4-benzo[d][1,2,3]triazin-3-ylethyl)]-3-(4-thien-3-yl-phenylthio) propionate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of tert-butyl-2-[2-(4-oxo-4-benzo[d][1,2,3]triazin-3-ylethyl)]-3-(4-thien-3-yl-phenylthio) propionate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of tert-butyl-2-[2-(4-oxo-4-benzo[d][1,2,3]triazin-3-ylethyl)]-3-(4-thien-3-yl-phenylthio) propionate

There total 8 articles about tert-butyl-2-[2-(4-oxo-4-benzo[d][1,2,3]triazin-3-ylethyl)]-3-(4-thien-3-yl-phenylthio) propionate 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:

: 97-65-4,25119-64-6
2-methylenesuccinic acid

: 427895-09-8
tert-butyl-2-[2-(4-oxo-4-benzo[d][1,2,3]triazin-3-ylethyl)]-3-(4-thien-3-yl-phenylthio) propionate

Guidance literature:: Multi-step reaction with 8 steps

1: 97 percent / Amberlyst 15 H⁺ resin / 72 h / 20 °C

2: 67.5 percent / H₂SO₄ / CH₂Cl₂ / 0 - 20 °C

3: 75.3 percent / LiOH / H₂O; dioxane / 2.5 h / 0 - 20 °C

4: 80.2 percent / NaOMe / methanol / 20 °C

5: N-methylmorpholine / 1,2-dimethoxy-ethane / 20 °C

6: 34 g / NaBH₄ / 1,2-dimethoxy-ethane; H₂O / 1 h / -10 °C

7: 88 percent / Ph₃P; DIAD / tetrahydrofuran / 1.5 h / 0 - 20 °C

8: 71 percent / LiCl / Pd(PPh₃)4 / toluene / Heating

With 4-methyl-morpholine; lithium hydroxide; sodium tetrahydroborate; di-isopropyl azodicarboxylate; Amberlyst 15 H⁺ resin; sulfuric acid; sodium methylate; triphenylphosphine; lithium chloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; methanol; 1,2-dimethoxyethane; dichloromethane; water; toluene; 7: Mitsunobu reaction / 8: Stille reaction;
DOI:10.1016/S0968-0896(01)00311-X

Reference yield:

: 7338-27-4
4-methoxy-2-methylene-4-oxobutanoic acid

: 427895-09-8
tert-butyl-2-[2-(4-oxo-4-benzo[d][1,2,3]triazin-3-ylethyl)]-3-(4-thien-3-yl-phenylthio) propionate

Guidance literature:: Multi-step reaction with 7 steps

1: 67.5 percent / H₂SO₄ / CH₂Cl₂ / 0 - 20 °C

2: 75.3 percent / LiOH / H₂O; dioxane / 2.5 h / 0 - 20 °C

3: 80.2 percent / NaOMe / methanol / 20 °C

4: N-methylmorpholine / 1,2-dimethoxy-ethane / 20 °C

5: 34 g / NaBH₄ / 1,2-dimethoxy-ethane; H₂O / 1 h / -10 °C

6: 88 percent / Ph₃P; DIAD / tetrahydrofuran / 1.5 h / 0 - 20 °C

7: 71 percent / LiCl / Pd(PPh₃)4 / toluene / Heating

With 4-methyl-morpholine; lithium hydroxide; sodium tetrahydroborate; di-isopropyl azodicarboxylate; sulfuric acid; sodium methylate; triphenylphosphine; lithium chloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; methanol; 1,2-dimethoxyethane; dichloromethane; water; toluene; 6: Mitsunobu reaction / 7: Stille reaction;
DOI:10.1016/S0968-0896(01)00311-X

Reference yield:

: 106-53-6
para-bromobenzenethiol

: 427895-09-8
tert-butyl-2-[2-(4-oxo-4-benzo[d][1,2,3]triazin-3-ylethyl)]-3-(4-thien-3-yl-phenylthio) propionate

Guidance literature:: Multi-step reaction with 5 steps

1: 80.2 percent / NaOMe / methanol / 20 °C

2: N-methylmorpholine / 1,2-dimethoxy-ethane / 20 °C

3: 34 g / NaBH₄ / 1,2-dimethoxy-ethane; H₂O / 1 h / -10 °C

4: 88 percent / Ph₃P; DIAD / tetrahydrofuran / 1.5 h / 0 - 20 °C

5: 71 percent / LiCl / Pd(PPh₃)4 / toluene / Heating

With 4-methyl-morpholine; sodium tetrahydroborate; di-isopropyl azodicarboxylate; sodium methylate; triphenylphosphine; lithium chloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; water; toluene; 4: Mitsunobu reaction / 5: Stille reaction;
DOI:10.1016/S0968-0896(01)00311-X