pivaloyloxymethyl (6-{(pyridin-2-ylsulfonyl)[4-(thiazol-2-yl)benzyl]aminomethyl}pyridin-2-ylamino)acetate

Base Information

Chemical Name:pivaloyloxymethyl (6-{(pyridin-2-ylsulfonyl)[4-(thiazol-2-yl)benzyl]aminomethyl}pyridin-2-ylamino)acetate
CAS No.:1273387-09-9
Molecular Formula:C₂₉H₃₁N₅O₆S₂
Molecular Weight:609.727
Hs Code.:

Synonyms:pivaloyloxymethyl (6-{(pyridin-2-ylsulfonyl)[4-(thiazol-2-yl)benzyl]aminomethyl}pyridin-2-ylamino)acetate

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Chemical Property of pivaloyloxymethyl (6-{(pyridin-2-ylsulfonyl)[4-(thiazol-2-yl)benzyl]aminomethyl}pyridin-2-ylamino)acetate

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Technology Process of pivaloyloxymethyl (6-{(pyridin-2-ylsulfonyl)[4-(thiazol-2-yl)benzyl]aminomethyl}pyridin-2-ylamino)acetate

There total 9 articles about pivaloyloxymethyl (6-{(pyridin-2-ylsulfonyl)[4-(thiazol-2-yl)benzyl]aminomethyl}pyridin-2-ylamino)acetate 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: 66.0%

: 18997-19-8
Chloromethyl pivalate

: 1187450-51-6
(6-{(pyridin-2-ylsulfonyl)[4-(thiazol-2-yl)benzyl]aminomethyl}pyridin-2-ylamino)-acetic acid

: 1273387-09-9
pivaloyloxymethyl (6-{(pyridin-2-ylsulfonyl)[4-(thiazol-2-yl)benzyl]aminomethyl}pyridin-2-ylamino)acetate

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 15h;

Reference yield:

: 203321-86-2
6-tert-butoxycarbonylamino-pyridine-2-carboxylic acid ethyl ester

: 1273387-09-9
pivaloyloxymethyl (6-{(pyridin-2-ylsulfonyl)[4-(thiazol-2-yl)benzyl]aminomethyl}pyridin-2-ylamino)acetate

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1.33 h / 20 °C / Inert atmosphere; Cooling with ice

1.2: 1.17 h / 20 °C / Cooling with ice

2.1: ethanol; calcium chloride; sodium tetrahydroborate / Tetraethylene glycol dimethyl ether / 35 °C / Cooling with ice

2.2: 1.17 h / 29 °C / Cooling with ice

3.1: tributylphosphine; diamide / tetrahydrofuran / 12 h / 20 °C

4.1: hydrogenchloride / 1,4-dioxane / 50 h / 20 °C

5.1: potassium carbonate / N,N-dimethyl-formamide / 15 h / 20 °C

With hydrogenchloride; sodium tetrahydroborate; ethanol; tributylphosphine; diamide; sodium hydride; potassium carbonate; calcium chloride; In tetrahydrofuran; 1,4-dioxane; Tetraethylene glycol dimethyl ether; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 454678-91-2
(4-(thiazol-2-yl)phenyl)methanol

: 1273387-09-9
pivaloyloxymethyl (6-{(pyridin-2-ylsulfonyl)[4-(thiazol-2-yl)benzyl]aminomethyl}pyridin-2-ylamino)acetate

Guidance literature:: Multi-step reaction with 7 steps

1: triphenylphosphine; N-Bromosuccinimide / tetrahydrofuran / 1.5 h / 20 °C

2: potassium carbonate / dichloromethane / 3 h / 20 °C

3: hydrogenchloride / 1,4-dioxane / 1 h / 20 °C

4: triethylamine / dichloromethane / 3 h / 20 °C

5: tributylphosphine; diamide / tetrahydrofuran / 12 h / 20 °C

6: hydrogenchloride / 1,4-dioxane / 50 h / 20 °C

7: potassium carbonate / N,N-dimethyl-formamide / 15 h / 20 °C

With hydrogenchloride; N-Bromosuccinimide; tributylphosphine; diamide; potassium carbonate; triethylamine; triphenylphosphine; In tetrahydrofuran; 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;