2-((S)-2-benzyloxy-1-tert-butoxycarbonylaminoethyl)oxazole-4-carboxylic acid

Base Information

Chemical Name:2-((S)-2-benzyloxy-1-tert-butoxycarbonylaminoethyl)oxazole-4-carboxylic acid
CAS No.:301662-03-3
Molecular Formula:C₁₈H₂₂N₂O₆
Molecular Weight:362.382
Hs Code.:

Synonyms:2-((S)-2-benzyloxy-1-tert-butoxycarbonylaminoethyl)oxazole-4-carboxylic acid

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Chemical Property of 2-((S)-2-benzyloxy-1-tert-butoxycarbonylaminoethyl)oxazole-4-carboxylic acid

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Technology Process of 2-((S)-2-benzyloxy-1-tert-butoxycarbonylaminoethyl)oxazole-4-carboxylic acid

There total 3 articles about 2-((S)-2-benzyloxy-1-tert-butoxycarbonylaminoethyl)oxazole-4-carboxylic acid 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:

: 1095973-66-2
2-[(1S)-1-[[(1,1-dimethylethoxy)carbonyl]amino]-2-(phenylmethoxy)ethyl]-2-(4S)-oxazoline methyl ester

: 301662-03-3
2-((S)-2-benzyloxy-1-tert-butoxycarbonylaminoethyl)oxazole-4-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: Bromotrichloromethane; 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 4 h / 0 - 20 °C

2: lithium hydroxide monohydrate; water / tetrahydrofuran; methanol / 8 h / 0 - 20 °C

With lithium hydroxide monohydrate; Bromotrichloromethane; water; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; methanol; dichloromethane;

Reference yield:

: 817625-25-5
(S)-2-((S)-3-benzyloxy-2-tert-butoxycarbonylaminopropionylamino)-3-hydroxypropionic acid methyl ester

: 301662-03-3
2-((S)-2-benzyloxy-1-tert-butoxycarbonylaminoethyl)oxazole-4-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: diethylamino-sulfur trifluoride / dichloromethane / 5 h / -78 °C / Inert atmosphere

2: Bromotrichloromethane; 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 4 h / 0 - 20 °C

3: lithium hydroxide monohydrate; water / tetrahydrofuran; methanol / 8 h / 0 - 20 °C

With lithium hydroxide monohydrate; Bromotrichloromethane; diethylamino-sulfur trifluoride; water; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; methanol; dichloromethane;

Reference yield:

: 23680-31-1
BOC-O-benzyl-L-serine

: 301662-03-3
2-((S)-2-benzyloxy-1-tert-butoxycarbonylaminoethyl)oxazole-4-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1: 4-methyl-morpholine; benzotriazol-1-ol; dicyclohexyl-carbodiimide / tetrahydrofuran / 24 h / 0 - 20 °C

2: diethylamino-sulfur trifluoride / dichloromethane / 5 h / -78 °C / Inert atmosphere

3: Bromotrichloromethane; 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 4 h / 0 - 20 °C

4: lithium hydroxide monohydrate; water / tetrahydrofuran; methanol / 8 h / 0 - 20 °C

With 4-methyl-morpholine; lithium hydroxide monohydrate; Bromotrichloromethane; diethylamino-sulfur trifluoride; water; benzotriazol-1-ol; 1,8-diazabicyclo[5.4.0]undec-7-ene; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; dichloromethane;