(R)-(1-(3-methoxy-4-(methylamino)-5-nitrobenzoyl)piperidin-3-yl)carbamic acid tert-butyl ester

Base Information

Chemical Name:(R)-(1-(3-methoxy-4-(methylamino)-5-nitrobenzoyl)piperidin-3-yl)carbamic acid tert-butyl ester
CAS No.:1549812-25-0
Molecular Formula:C₁₉H₂₈N₄O₆
Molecular Weight:408.455
Hs Code.:

Synonyms:(R)-(1-(3-methoxy-4-(methylamino)-5-nitrobenzoyl)piperidin-3-yl)carbamic acid tert-butyl ester

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Chemical Property of (R)-(1-(3-methoxy-4-(methylamino)-5-nitrobenzoyl)piperidin-3-yl)carbamic acid tert-butyl ester

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Technology Process of (R)-(1-(3-methoxy-4-(methylamino)-5-nitrobenzoyl)piperidin-3-yl)carbamic acid tert-butyl ester

There total 5 articles about (R)-(1-(3-methoxy-4-(methylamino)-5-nitrobenzoyl)piperidin-3-yl)carbamic acid tert-butyl 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: 100.0%

: 309956-78-3,172603-05-3
(R)-piperidin-3-ylcarbamic acid tert-butyl ester

: 1549812-23-8
3-methoxy-4-(methylamino)-5-nitrobenzoic acid

: 1549812-25-0
(R)-(1-(3-methoxy-4-(methylamino)-5-nitrobenzoyl)piperidin-3-yl)carbamic acid tert-butyl ester

Guidance literature:: 3-methoxy-4-(methylamino)-5-nitrobenzoic acid; With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In tetrahydrofuran; N,N-dimethyl-formamide; for 0.666667h; Cooling with ice;

(R)-piperidin-3-ylcarbamic acid tert-butyl ester; In tetrahydrofuran; N,N-dimethyl-formamide; at 20 ℃; for 10h; Solvent; Temperature;

Reference yield:

: 1549812-20-5
methyl 3-methoxy-4-(methylamino)-5-nitrobenzoate

: 1549812-25-0
(R)-(1-(3-methoxy-4-(methylamino)-5-nitrobenzoyl)piperidin-3-yl)carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: lithium hydroxide / tetrahydrofuran; water / 19 h / 20 °C

1.2: pH Ca_. 4

2.1: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide / 0.5 h

2.2: 1.5 h

With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; lithium hydroxide; In tetrahydrofuran; water; N,N-dimethyl-formamide;

Reference yield:

: 63603-09-8
methyl 4-chloro-3-methoxy-5-nitrobenzoate

: 1549812-25-0
(R)-(1-(3-methoxy-4-(methylamino)-5-nitrobenzoyl)piperidin-3-yl)carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: tetrahydrofuran; N,N-dimethyl-formamide / 3 h / 0 - 80 °C

2.1: lithium hydroxide / tetrahydrofuran; water / 19 h / 20 °C

2.2: pH Ca_. 4

3.1: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide / 0.5 h

3.2: 1.5 h

With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; lithium hydroxide; In tetrahydrofuran; water; N,N-dimethyl-formamide;