(2-Amino-4-benzyloxy-5-methoxy-phenyl)-((S)-2-hydroxymethyl-azetidin-1-yl)-methanone

Base Information

Chemical Name:(2-Amino-4-benzyloxy-5-methoxy-phenyl)-((S)-2-hydroxymethyl-azetidin-1-yl)-methanone
CAS No.:195607-09-1
Molecular Formula:C₁₉H₂₂N₂O₄
Molecular Weight:342.395
Hs Code.:

Synonyms:(2-Amino-4-benzyloxy-5-methoxy-phenyl)-((S)-2-hydroxymethyl-azetidin-1-yl)-methanone

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Chemical Property of (2-Amino-4-benzyloxy-5-methoxy-phenyl)-((S)-2-hydroxymethyl-azetidin-1-yl)-methanone

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Technology Process of (2-Amino-4-benzyloxy-5-methoxy-phenyl)-((S)-2-hydroxymethyl-azetidin-1-yl)-methanone

There total 5 articles about (2-Amino-4-benzyloxy-5-methoxy-phenyl)-((S)-2-hydroxymethyl-azetidin-1-yl)-methanone 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:

: 64154-78-5
4-benzyloxy-5-methoxy-2-nitrobenzoyl chloride

: 195607-09-1
(2-Amino-4-benzyloxy-5-methoxy-phenyl)-((S)-2-hydroxymethyl-azetidin-1-yl)-methanone

Guidance literature:: Multi-step reaction with 4 steps

1: Et₃N

2: SOCl₂

3: 78 percent / lithium borohydride / tetrahydrofuran / 0 - 20 °C

4: SnCl₂*2H₂O

With lithium borohydride; thionyl chloride; triethylamine; tin(ll) chloride; In tetrahydrofuran;
DOI:10.1016/S0040-4039(97)01297-5

Reference yield:

: 60547-92-4
4-(benzyloxy)-5-methoxy-2-nitrobenzoic acid

: 195607-09-1
(2-Amino-4-benzyloxy-5-methoxy-phenyl)-((S)-2-hydroxymethyl-azetidin-1-yl)-methanone

Guidance literature:: Multi-step reaction with 5 steps

1: oxalyl chloride / tetrahydrofuran

2: Et₃N

3: SOCl₂

4: 78 percent / lithium borohydride / tetrahydrofuran / 0 - 20 °C

5: SnCl₂*2H₂O

With lithium borohydride; thionyl chloride; oxalyl dichloride; triethylamine; tin(ll) chloride; In tetrahydrofuran;
DOI:10.1016/S0040-4039(97)01297-5

Reference yield:

: 195607-02-4
(S)-1-(4-Benzyloxy-5-methoxy-2-nitro-benzoyl)-azetidine-2-carboxylic acid

: 195607-09-1
(2-Amino-4-benzyloxy-5-methoxy-phenyl)-((S)-2-hydroxymethyl-azetidin-1-yl)-methanone

Guidance literature:: Multi-step reaction with 3 steps

1: SOCl₂

2: 78 percent / lithium borohydride / tetrahydrofuran / 0 - 20 °C

3: SnCl₂*2H₂O

With lithium borohydride; thionyl chloride; tin(ll) chloride; In tetrahydrofuran;
DOI:10.1016/S0040-4039(97)01297-5