(3R,4R)-4-[4-(2-fluoro-3-methoxy-6-methoxymethoxybenzoyl)benzyloxy]-3-[(pyridine-4-carbonyl)amino]azepane-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:(3R,4R)-4-[4-(2-fluoro-3-methoxy-6-methoxymethoxybenzoyl)benzyloxy]-3-[(pyridine-4-carbonyl)amino]azepane-1-carboxylic acid tert-butyl ester
CAS No.:677323-89-6
Molecular Formula:C₃₄H₄₀FN₃O₈
Molecular Weight:637.705
Hs Code.:

Synonyms:(3R,4R)-4-[4-(2-fluoro-3-methoxy-6-methoxymethoxybenzoyl)benzyloxy]-3-[(pyridine-4-carbonyl)amino]azepane-1-carboxylic acid tert-butyl ester

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Chemical Property of (3R,4R)-4-[4-(2-fluoro-3-methoxy-6-methoxymethoxybenzoyl)benzyloxy]-3-[(pyridine-4-carbonyl)amino]azepane-1-carboxylic acid tert-butyl ester

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Technology Process of (3R,4R)-4-[4-(2-fluoro-3-methoxy-6-methoxymethoxybenzoyl)benzyloxy]-3-[(pyridine-4-carbonyl)amino]azepane-1-carboxylic acid tert-butyl ester

There total 7 articles about (3R,4R)-4-[4-(2-fluoro-3-methoxy-6-methoxymethoxybenzoyl)benzyloxy]-3-[(pyridine-4-carbonyl)amino]azepane-1-carboxylic acid tert-butyl 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:

: 677323-88-5
(3R,4R)-4-{4-[(2-fluoro-3-methoxy-6-methoxymethoxyphenyl)-(1,1,1-triisopropylsilanyloxy)methyl]benzyloxy}-3-[(pyridine-4-carbonyl)amino]azepane-1-carboxylic acid tert-butyl ester

: 677323-89-6
(3R,4R)-4-[4-(2-fluoro-3-methoxy-6-methoxymethoxybenzoyl)benzyloxy]-3-[(pyridine-4-carbonyl)amino]azepane-1-carboxylic acid tert-butyl ester

Guidance literature:: (3R,4R)-4-{4-[(2-fluoro-3-methoxy-6-methoxymethoxyphenyl)-(1,1,1-triisopropylsilanyloxy)methyl]benzyloxy}-3-[(pyridine-4-carbonyl)amino]azepane-1-carboxylic acid tert-butyl ester; With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 15h;

With manganese(IV) oxide; In dichloromethane; at 20 ℃; for 24h;
DOI:10.1021/jm0310479

Reference yield:

: 55-22-1
pyridine-4-carboxylic acid

: 677323-89-6
(3R,4R)-4-[4-(2-fluoro-3-methoxy-6-methoxymethoxybenzoyl)benzyloxy]-3-[(pyridine-4-carbonyl)amino]azepane-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: 92 percent / DMAP; DCC / CH₂Cl₂ / 15 h / 20 °C

2.1: Bu₄NF*4H₂O / tetrahydrofuran / 15 h / 20 °C

2.2: MnO₂ / CH₂Cl₂ / 24 h / 20 °C

With dmap; tetrabutyl ammonium fluoride; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm0310479

Reference yield:

: 677323-83-0
4-[(2-fluoro-3-methoxy-6-methoxymethoxy-phenyl)-hydroxy-methyl]-benzoicacidmethylester

: 677323-89-6
(3R,4R)-4-[4-(2-fluoro-3-methoxy-6-methoxymethoxybenzoyl)benzyloxy]-3-[(pyridine-4-carbonyl)amino]azepane-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: imidazole / dimethylformamide / 15 h / 20 °C

1.2: 90 percent / TIPSOSO₂CF₃ / dimethylformamide / 36 h / 100 °C

2.1: 70 percent / LiAlH₄ / tetrahydrofuran / 3 h / 20 °C

3.1: 74 percent / PPh₃; CCl₄ / 3 h / 20 °C

4.1: 43 percent / tetrahydrofuran / 2 h / Heating

5.1: 92 percent / DMAP; DCC / CH₂Cl₂ / 15 h / 20 °C

6.1: Bu₄NF*4H₂O / tetrahydrofuran / 15 h / 20 °C

6.2: MnO₂ / CH₂Cl₂ / 24 h / 20 °C

With 1H-imidazole; tetrachloromethane; dmap; lithium aluminium tetrahydride; tetrabutyl ammonium fluoride; dicyclohexyl-carbodiimide; triphenylphosphine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm0310479