tert-butyl [tert-butoxycarbonyl(6-{(2-fluorobenzenesulfonyl) [4-(1,1-dimethylpentyl)benzyl]aminomethyl}pyridin-2-yl)amino]acetate

Base Information

Chemical Name:tert-butyl [tert-butoxycarbonyl(6-{(2-fluorobenzenesulfonyl) [4-(1,1-dimethylpentyl)benzyl]aminomethyl}pyridin-2-yl)amino]acetate
CAS No.:1313217-28-5
Molecular Formula:C₃₇H₅₀FN₃O₆S
Molecular Weight:683.885
Hs Code.:

Synonyms:tert-butyl [tert-butoxycarbonyl(6-{(2-fluorobenzenesulfonyl) [4-(1,1-dimethylpentyl)benzyl]aminomethyl}pyridin-2-yl)amino]acetate

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Chemical Property of tert-butyl [tert-butoxycarbonyl(6-{(2-fluorobenzenesulfonyl) [4-(1,1-dimethylpentyl)benzyl]aminomethyl}pyridin-2-yl)amino]acetate

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Technology Process of tert-butyl [tert-butoxycarbonyl(6-{(2-fluorobenzenesulfonyl) [4-(1,1-dimethylpentyl)benzyl]aminomethyl}pyridin-2-yl)amino]acetate

There total 10 articles about tert-butyl [tert-butoxycarbonyl(6-{(2-fluorobenzenesulfonyl) [4-(1,1-dimethylpentyl)benzyl]aminomethyl}pyridin-2-yl)amino]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: 70.0%

: 2905-21-7
2-fluorobenzenesulfonyl chloride

: 1313217-95-6
tert-butyl [tert-butoxycarbonyl(6-{[4-(1,1-dimethylpentyl)benzyl]aminomethyl}pyridin-2-yl)amino]acetate

: 1313217-28-5
tert-butyl [tert-butoxycarbonyl(6-{(2-fluorobenzenesulfonyl) [4-(1,1-dimethylpentyl)benzyl]aminomethyl}pyridin-2-yl)amino]acetate

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 6h;

Reference yield:

: 5292-43-3
bromoacetic acid tert-butyl ester

: 1313217-28-5
tert-butyl [tert-butoxycarbonyl(6-{(2-fluorobenzenesulfonyl) [4-(1,1-dimethylpentyl)benzyl]aminomethyl}pyridin-2-yl)amino]acetate

Guidance literature:: Multi-step reaction with 7 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: calcium chloride; potassium borohydride / Tetraethylene glycol dimethyl ether; ethanol / 0.92 h / 20 - 35 °C / Cooling with ice

2.2: 1.17 h / 20 °C / Cooling with ice

3.1: Dess-Martin periodane / dichloromethane / 2.33 h / Cooling with ice; Inert atmosphere

4.1: hydroxylamine hydrochloride; pyridine / methanol / 1 h / 20 °C

5.1: hydrogen / palladium 10% on activated carbon / ethanol; water / 1 h / 20 °C / 760.05 Torr

6.1: dichloromethane / 18 h / 20 °C

6.2: 18 h / 20 °C

7.1: triethylamine / dichloromethane / 6 h / 20 °C

With pyridine; potassium borohydride; hydroxylamine hydrochloride; hydrogen; sodium hydride; Dess-Martin periodane; triethylamine; calcium chloride; palladium 10% on activated carbon; In methanol; ethanol; dichloromethane; Tetraethylene glycol dimethyl ether; water; N,N-dimethyl-formamide; mineral oil;

Reference yield:

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

: 1313217-28-5
tert-butyl [tert-butoxycarbonyl(6-{(2-fluorobenzenesulfonyl) [4-(1,1-dimethylpentyl)benzyl]aminomethyl}pyridin-2-yl)amino]acetate

Guidance literature:: Multi-step reaction with 7 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: calcium chloride; potassium borohydride / Tetraethylene glycol dimethyl ether; ethanol / 0.92 h / 20 - 35 °C / Cooling with ice

2.2: 1.17 h / 20 °C / Cooling with ice

3.1: Dess-Martin periodane / dichloromethane / 2.33 h / Cooling with ice; Inert atmosphere

4.1: hydroxylamine hydrochloride; pyridine / methanol / 1 h / 20 °C

5.1: hydrogen / palladium 10% on activated carbon / ethanol; water / 1 h / 20 °C / 760.05 Torr

6.1: dichloromethane / 18 h / 20 °C

6.2: 18 h / 20 °C

7.1: triethylamine / dichloromethane / 6 h / 20 °C

With pyridine; potassium borohydride; hydroxylamine hydrochloride; hydrogen; sodium hydride; Dess-Martin periodane; triethylamine; calcium chloride; palladium 10% on activated carbon; In methanol; ethanol; dichloromethane; Tetraethylene glycol dimethyl ether; water; N,N-dimethyl-formamide; mineral oil;