4-[5-allyloxycarbonylamino-4-((2S)-2-hydroxymethylpyrrolidine-1-carbonyl)-2-methoxyphenoxy]butanoic acid methyl ester

Base Information

Chemical Name:4-[5-allyloxycarbonylamino-4-((2S)-2-hydroxymethylpyrrolidine-1-carbonyl)-2-methoxyphenoxy]butanoic acid methyl ester
CAS No.:909415-16-3
Molecular Formula:C₂₂H₃₀N₂O₈
Molecular Weight:450.489
Hs Code.:

Synonyms:4-[5-allyloxycarbonylamino-4-((2S)-2-hydroxymethylpyrrolidine-1-carbonyl)-2-methoxyphenoxy]butanoic acid methyl ester

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Chemical Property of 4-[5-allyloxycarbonylamino-4-((2S)-2-hydroxymethylpyrrolidine-1-carbonyl)-2-methoxyphenoxy]butanoic acid methyl ester

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Technology Process of 4-[5-allyloxycarbonylamino-4-((2S)-2-hydroxymethylpyrrolidine-1-carbonyl)-2-methoxyphenoxy]butanoic acid methyl ester

There total 9 articles about 4-[5-allyloxycarbonylamino-4-((2S)-2-hydroxymethylpyrrolidine-1-carbonyl)-2-methoxyphenoxy]butanoic acid methyl 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%

: 909415-15-2
4-[5-amino-4-((2S)-2-hydroxymethylpyrrolidine-1-carbonyl)-2-methoxyphenoxy]butanoic acid methyl ester

: 2937-50-0
Allyl chloroformate

: 909415-16-3
4-[5-allyloxycarbonylamino-4-((2S)-2-hydroxymethylpyrrolidine-1-carbonyl)-2-methoxyphenoxy]butanoic acid methyl ester

Guidance literature:: With pyridine; In dichloromethane; at 0 - 20 ℃;

Reference yield:

: 909415-14-1
4-[4-((2S)-2-hydroxymethylpyrrolidine-1-carbonyl)-2-methoxy-5-nitrophenoxy]butanoic acid methyl ester

: 909415-16-3
4-[5-allyloxycarbonylamino-4-((2S)-2-hydroxymethylpyrrolidine-1-carbonyl)-2-methoxyphenoxy]butanoic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / H₂ / Pd/C / ethanol / 2068.59 Torr

2: 27 g / pyridine / CH₂Cl₂ / 18 h / 20 °C

With pyridine; hydrogen; palladium on activated charcoal; In ethanol; dichloromethane;
DOI:10.1021/jm051199z

Reference yield:

: 4897-84-1
Methyl 4-bromobutyrate

: 909415-16-3
4-[5-allyloxycarbonylamino-4-((2S)-2-hydroxymethylpyrrolidine-1-carbonyl)-2-methoxyphenoxy]butanoic acid methyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 85 percent / K₂CO₃ / dimethylformamide / 16 h / 20 °C

2: Ac₂O; aq. HNO₃ / 2.5 h / 0 °C

3: 31 g / aq. KMnO₄ / acetone / 1 h

4: (COCl)2; DMF / CH₂Cl₂ / 18 h / 20 °C

5: 100 percent / Et₃N / CH₂Cl₂ / -30 - 20 °C

6: 100 percent / H₂ / Pd/C / ethanol / 2068.59 Torr

7: 27 g / pyridine / CH₂Cl₂ / 18 h / 20 °C

With pyridine; potassium permanganate; oxalyl dichloride; hydrogen; nitric acid; acetic anhydride; potassium carbonate; triethylamine; N,N-dimethyl-formamide; palladium on activated charcoal; In ethanol; dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jm051199z