(1S,3R,4R)-2-(4-tert-butylphenylsulfonyl)-2-azabicyclo[2.2.1]heptane-3-carboxylic acid methyl ester

Base Information

• Chemical Name: (1S,3R,4R)-2-(4-tert-butylphenylsulfonyl)-2-azabicyclo[2.2.1]heptane-3-carboxylic acid methyl ester
• CAS No.: 297143-32-9
• Molecular Formula: C₁₈H₂₅NO₄S
• Molecular Weight: 351.467
• Mol file: 297143-32-9.mol

Synonyms:(1S,3R,4R)-2-(4-tert-butylphenylsulfonyl)-2-azabicyclo[2.2.1]heptane-3-carboxylic acid methyl ester

Chemical Property of (1S,3R,4R)-2-(4-tert-butylphenylsulfonyl)-2-azabicyclo[2.2.1]heptane-3-carboxylic acid methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (1S,3R,4R)-2-(4-tert-butylphenylsulfonyl)-2-azabicyclo[2.2.1]heptane-3-carboxylic acid methyl ester

There total 3 articles about (1S,3R,4R)-2-(4-tert-butylphenylsulfonyl)-2-azabicyclo[2.2.1]heptane-3-carboxylic 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: 80.0%

4-tert-butylbenzenesulfonyl chloride (15084-51-2) + (1S,3R,4R)-2-azabicyclo[2.2.1]heptane-3-carboxylic acid methyl ester (297143-31-8,220093-41-4) → (1S,3R,4R)-2-(4-tert-butylphenylsulfonyl)-2-azabicyclo[2.2.1]heptane-3-carboxylic acid methyl ester (297143-32-9)

Guidance literature:

With triethylamine; In dichloromethane; at 20 ℃; for 2h;

DOI:10.1016/S0022-328X(00)00025-5

Reference yield:

(1R,3R,4S)-2-[(1S)-1-phenylethyl]-2-azabicyclo[2.2.1]hept-5-ene-3-carboxylic acid methyl ester (130195-74-3) → (1S,3R,4R)-2-(4-tert-butylphenylsulfonyl)-2-azabicyclo[2.2.1]heptane-3-carboxylic acid methyl ester (297143-32-9)

Guidance literature:

Multi-step reaction with 2 steps

1: H₂

2: 80 percent / Et₃N / CH₂Cl₂ / 2 h / 20 °C

With hydrogen; triethylamine; In dichloromethane;

DOI:10.1016/S0022-328X(00)00025-5

Reference yield:

cyclopenta-1,3-diene (542-92-7,25568-84-7,7313-32-8) → (1S,3R,4R)-2-(4-tert-butylphenylsulfonyl)-2-azabicyclo[2.2.1]heptane-3-carboxylic acid methyl ester (297143-32-9)

Guidance literature:

Multi-step reaction with 3 steps

1: H₂

2: 80 percent / Et₃N / CH₂Cl₂ / 2 h / 20 °C

With hydrogen; triethylamine; In dichloromethane; 1: aza-Diels-Alder reaction;

DOI:10.1016/S0022-328X(00)00025-5

upstream raw materials:

4-tert-butylbenzenesulfonyl chloride

(1S,3R,4R)-2-azabicyclo[2.2.1]heptane-3-carboxylic acid methyl ester

(1R,3R,4S)-2-[(1S)-1-phenylethyl]-2-azabicyclo[2.2.1]hept-5-ene-3-carboxylic acid methyl ester

cyclopenta-1,3-diene

Downstream raw materials:

(1S,3R,4R)-2-(p-tert-butylphenylsulphonyl)-2-aza-bicyclo[2.2.1]heptane-3-caboxylic acid