(S)-6-(benzyloxy)methyl-2-{2-[1-(tert-butoxycarbonyl)aminoethyl]-5-methyloxazol-4-yl}pyridine-3-carboxylic acid

Base Information

Chemical Name:(S)-6-(benzyloxy)methyl-2-{2-[1-(tert-butoxycarbonyl)aminoethyl]-5-methyloxazol-4-yl}pyridine-3-carboxylic acid
CAS No.:205648-21-1
Molecular Formula:C₂₅H₂₉N₃O₆
Molecular Weight:467.522
Hs Code.:

Synonyms:(S)-6-(benzyloxy)methyl-2-{2-[1-(tert-butoxycarbonyl)aminoethyl]-5-methyloxazol-4-yl}pyridine-3-carboxylic acid

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Chemical Property of (S)-6-(benzyloxy)methyl-2-{2-[1-(tert-butoxycarbonyl)aminoethyl]-5-methyloxazol-4-yl}pyridine-3-carboxylic acid

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Technology Process of (S)-6-(benzyloxy)methyl-2-{2-[1-(tert-butoxycarbonyl)aminoethyl]-5-methyloxazol-4-yl}pyridine-3-carboxylic acid

There total 9 articles about (S)-6-(benzyloxy)methyl-2-{2-[1-(tert-butoxycarbonyl)aminoethyl]-5-methyloxazol-4-yl}pyridine-3-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: 92.0%

: 205648-20-0
(S)-ethyl 6-(benzyloxy)methyl-2-{2-[1-(tert-butoxycarbonyl)aminoethyl]-5-methyloxazol-4-yl}pyridine-3-carboxylate

: 205648-21-1
(S)-6-(benzyloxy)methyl-2-{2-[1-(tert-butoxycarbonyl)aminoethyl]-5-methyloxazol-4-yl}pyridine-3-carboxylic acid

Guidance literature:: With lithium hydroxide; In tetrahydrofuran;
DOI:10.1055/s-1998-1670

Reference yield:

: 78981-25-6,81587-17-9,85642-13-3
tert-butyl (1S)-2-amino-1-methyl-2-oxoethylcarbamate

: 205648-21-1
(S)-6-(benzyloxy)methyl-2-{2-[1-(tert-butoxycarbonyl)aminoethyl]-5-methyloxazol-4-yl}pyridine-3-carboxylic acid

Guidance literature:: Multi-step reaction with 9 steps

1: 80 percent / dirhodium(II) acetate / CHCl₃ / Heating

2: 70 percent / triethylamine; triphenylphosphine; iodine / CH₂Cl₂ / 20 °C

3: 95 percent / aq. LiOH / methanol / 5 h / 20 °C

4: triethylamine / tetrahydrofuran / 0.33 h / 0 °C

5: tetrahydrofuran / 20 °C

6: 85 percent / ammonium acetate / benzene; acetic acid / 24 h / Heating

7: ethanol / 50 °C

8: 0.5 h / 140 °C

9: 92 percent / aq. LiOH / tetrahydrofuran / 20 - 45 °C

With ammonium acetate; lithium hydroxide; iodine; triethylamine; triphenylphosphine; dirhodium tetraacetate; In tetrahydrofuran; methanol; ethanol; dichloromethane; chloroform; acetic acid; benzene; 1: Condensation / 2: Cyclization / 3: Hydrolysis / 4: Carboxylation / 5: Substitution / 6: Amination / 7: Condensation / 8: Cyclization / 9: Hydrolysis;
DOI:10.1021/ja994247b

Reference yield:

: 205648-17-5
(S)-2-[1-(tert-butoxycarbonyl)aminoethyl]-5-methyloxazole-4-carboxylic acid

: 205648-21-1
(S)-6-(benzyloxy)methyl-2-{2-[1-(tert-butoxycarbonyl)aminoethyl]-5-methyloxazol-4-yl}pyridine-3-carboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1: triethylamine / tetrahydrofuran / 0.33 h / 0 °C

2: tetrahydrofuran / 20 °C

3: 85 percent / ammonium acetate / benzene; acetic acid / 24 h / Heating

4: ethanol / 50 °C

5: 0.5 h / 140 °C

6: 92 percent / aq. LiOH / tetrahydrofuran / 20 - 45 °C

With ammonium acetate; lithium hydroxide; triethylamine; In tetrahydrofuran; ethanol; acetic acid; benzene; 1: Carboxylation / 2: Substitution / 3: Amination / 4: Condensation / 5: Cyclization / 6: Hydrolysis;
DOI:10.1021/ja994247b