benzyl <<4(S)-methyl-3(S)-(N-Boc-4-(benzyloxy)-D-phenylglycyl)-2-oxo-1-azetidinyl>oxy>acetate

Base Information

Chemical Name:benzyl <<4(S)-methyl-3(S)-(N-Boc-4-(benzyloxy)-D-phenylglycyl)-2-oxo-1-azetidinyl>oxy>acetate
CAS No.:131080-81-4
Molecular Formula:C₃₃H₃₇N₃O₈
Molecular Weight:603.672
Hs Code.:

Synonyms:benzyl <<4(S)-methyl-3(S)-(N-Boc-4-(benzyloxy)-D-phenylglycyl)-2-oxo-1-azetidinyl>oxy>acetate

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Chemical Property of benzyl <<4(S)-methyl-3(S)-(N-Boc-4-(benzyloxy)-D-phenylglycyl)-2-oxo-1-azetidinyl>oxy>acetate

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Technology Process of benzyl <<4(S)-methyl-3(S)-(N-Boc-4-(benzyloxy)-D-phenylglycyl)-2-oxo-1-azetidinyl>oxy>acetate

There total 5 articles about benzyl <<4(S)-methyl-3(S)-(N-Boc-4-(benzyloxy)-D-phenylglycyl)-2-oxo-1-azetidinyl>oxy>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:

: 24424-99-5
di-tert-butyl dicarbonate

: 131080-81-4
benzyl <<4(S)-methyl-3(S)-(N-Boc-4-(benzyloxy)-D-phenylglycyl)-2-oxo-1-azetidinyl>oxy>acetate

Guidance literature:: Multi-step reaction with 3 steps

1: 46 percent / potassium bicarbonate / ethyl acetate; tetrahydrofuran / 35 h

2: 76 percent / dicyclohexylcarbodiimide (DCC) / tetrahydrofuran

3: potassium bicarbonate / ethyl acetate; H₂O

With potassium hydrogencarbonate; dicyclohexyl-carbodiimide; In tetrahydrofuran; water; ethyl acetate;
DOI:10.1021/jm00107a014

Reference yield:

: 69489-40-3
D-2-[p-(benzyloxy)phenyl]glycine

: 131080-81-4
benzyl <<4(S)-methyl-3(S)-(N-Boc-4-(benzyloxy)-D-phenylglycyl)-2-oxo-1-azetidinyl>oxy>acetate

Guidance literature:: Multi-step reaction with 3 steps

1: 46 percent / potassium bicarbonate / ethyl acetate; tetrahydrofuran / 35 h

2: 76 percent / dicyclohexylcarbodiimide (DCC) / tetrahydrofuran

3: potassium bicarbonate / ethyl acetate; H₂O

With potassium hydrogencarbonate; dicyclohexyl-carbodiimide; In tetrahydrofuran; water; ethyl acetate;
DOI:10.1021/jm00107a014

Reference yield:

: 127526-64-1
(R)-(4-benzyloxyphenyl)(tert-butoxycarbonylamino)acetic acid

: 131080-81-4
benzyl <<4(S)-methyl-3(S)-(N-Boc-4-(benzyloxy)-D-phenylglycyl)-2-oxo-1-azetidinyl>oxy>acetate

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / dicyclohexylcarbodiimide (DCC) / tetrahydrofuran

2: potassium bicarbonate / ethyl acetate; H₂O

With potassium hydrogencarbonate; dicyclohexyl-carbodiimide; In tetrahydrofuran; water; ethyl acetate;
DOI:10.1021/jm00107a014