(S)-3-(4-phenyl-1H-imidazol-2-yl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

Base Information

• Chemical Name: (S)-3-(4-phenyl-1H-imidazol-2-yl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester
• CAS No.: 422572-63-2
• Molecular Formula: C₂₃H₂₅N₃O₂
• Molecular Weight: 375.47

Synonyms:(S)-3-(4-phenyl-1H-imidazol-2-yl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

Chemical Property of (S)-3-(4-phenyl-1H-imidazol-2-yl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

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Technology Process of (S)-3-(4-phenyl-1H-imidazol-2-yl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

There total 3 articles about (S)-3-(4-phenyl-1H-imidazol-2-yl)-3,4-dihydro-1H-isoquinoline-2-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:

(S)-3-(2-oxo-2-phenyl-ethylcarbamoyl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester (209526-36-3) → (S)-3-(4-phenyl-1H-imidazol-2-yl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester (422572-63-2)

Guidance literature:

With ammonium acetate; acetic acid; Heating;

DOI:10.1021/jm030548r

Reference yield:

(3S)-2-tert-butoxycarbonyl-1,2,3,4-tetrahydroisoquinole-3-carboxylic acid (115962-35-1,144069-68-1,78879-20-6) → (S)-3-(4-phenyl-1H-imidazol-2-yl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester (422572-63-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide; 1-hydroxybenzotriazole; N-methylmorpholine / CH₂Cl₂ / 72 h / 20 °C

2: NH₄OAc; AcOH / Heating

With 4-methyl-morpholine; ammonium acetate; benzotriazol-1-ol; acetic acid; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In dichloromethane;

DOI:10.1021/jm030548r

Reference yield:

2-Aminoacetophenone (613-89-8) → (S)-3-(4-phenyl-1H-imidazol-2-yl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester (422572-63-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide; 1-hydroxybenzotriazole; N-methylmorpholine / CH₂Cl₂ / 72 h / 20 °C

2: NH₄OAc; AcOH / Heating

With 4-methyl-morpholine; ammonium acetate; benzotriazol-1-ol; acetic acid; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In dichloromethane;

DOI:10.1021/jm030548r

upstream raw materials:

(S)-3-(2-oxo-2-phenyl-ethylcarbamoyl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

(3S)-2-tert-butoxycarbonyl-1,2,3,4-tetrahydroisoquinole-3-carboxylic acid

2-Aminoacetophenone

Downstream raw materials:

[2-[(3S)-3-(4-bromo-5-phenyl-1H-imidazol-2-yl)-3,4-dihydro-1H-isoquinolin-2-yl]-(1S)-1-(4-tert-butoxybenzyl)-2-oxo-ethyl]carbamic acid tert-butyl ester

[(1S)-1-(4-tert-butoxybenzyl)-2-oxo-2-[(3S)-3-(4-phenyl-1H-imidazol-2-yl)-3,4-dihydro-1H-isoquinolin-2-yl]ethyl]carbamic acid tert-butyl ester

(S)-3-(4-phenyl-1H-imidazol-2-yl)-1,2,3,4-tetrahydroisoquinoline

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