[(1S,2R)-2-((S)-1-Azido-propyl)-1-phenyl-cyclopropyl]-piperidin-1-yl-methanone

Base Information

Chemical Name:[(1S,2R)-2-((S)-1-Azido-propyl)-1-phenyl-cyclopropyl]-piperidin-1-yl-methanone
CAS No.:459143-57-8
Molecular Formula:C₁₈H₂₄N₄O
Molecular Weight:312.415
Hs Code.:

Synonyms:[(1S,2R)-2-((S)-1-Azido-propyl)-1-phenyl-cyclopropyl]-piperidin-1-yl-methanone

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Chemical Property of [(1S,2R)-2-((S)-1-Azido-propyl)-1-phenyl-cyclopropyl]-piperidin-1-yl-methanone

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Technology Process of [(1S,2R)-2-((S)-1-Azido-propyl)-1-phenyl-cyclopropyl]-piperidin-1-yl-methanone

There total 5 articles about [(1S,2R)-2-((S)-1-Azido-propyl)-1-phenyl-cyclopropyl]-piperidin-1-yl-methanone 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: 78.0%

: 459143-51-2
[(1S,2R)-2-((S)-1-Hydroxy-propyl)-1-phenyl-cyclopropyl]-piperidin-1-yl-methanone

: 459143-57-8
[(1S,2R)-2-((S)-1-Azido-propyl)-1-phenyl-cyclopropyl]-piperidin-1-yl-methanone

Guidance literature:: [(1S,2R)-2-((S)-1-Hydroxy-propyl)-1-phenyl-cyclopropyl]-piperidin-1-yl-methanone; With carbon tetrabromide; triphenylphosphine; In N,N,N,N,N,N-hexamethylphosphoric triamide; at 0 ℃; for 0.5h;

With sodium azide; In N,N,N,N,N,N-hexamethylphosphoric triamide; at 20 ℃; for 6h;
DOI:10.1016/S0968-0896(02)00030-5

Reference yield:

: 110-89-4
piperidine

: 459143-57-8
[(1S,2R)-2-((S)-1-Azido-propyl)-1-phenyl-cyclopropyl]-piperidin-1-yl-methanone

Guidance literature:: Multi-step reaction with 4 steps

1.1: 95 percent / AlCl₃ / CH₂Cl₂ / 24 h / 20 °C

2.1: 96 percent / (COCl)2; DMSO; Et₃N / CH₂Cl₂ / -78 °C

3.1: 94 percent / tetrahydrofuran; diethyl ether / 3 h / -15 °C

4.1: PPh₃CBr₄ / hexamethylphosphoric acid triamide / 0.5 h / 0 °C

4.2: 78 percent / NaN₃ / hexamethylphosphoric acid triamide / 6 h / 20 °C

With aluminium trichloride; oxalyl dichloride; carbon tetrabromide; dimethyl sulfoxide; triethylamine; triphenylphosphine; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; diethyl ether; dichloromethane; 2.1: Swern oxidation / 3.1: Grignard reaction;
DOI:10.1016/S0968-0896(02)00030-5

Reference yield:

: 63106-93-4,96847-52-8,96847-75-5,96847-53-9
(1S,5R)-1-phenyl-3-oxabicyclo[3.1.0]hexan-2-one

: 459143-57-8
[(1S,2R)-2-((S)-1-Azido-propyl)-1-phenyl-cyclopropyl]-piperidin-1-yl-methanone

Guidance literature:: Multi-step reaction with 4 steps

1.1: 95 percent / AlCl₃ / CH₂Cl₂ / 24 h / 20 °C

2.1: 96 percent / (COCl)2; DMSO; Et₃N / CH₂Cl₂ / -78 °C

3.1: 94 percent / tetrahydrofuran; diethyl ether / 3 h / -15 °C

4.1: PPh₃CBr₄ / hexamethylphosphoric acid triamide / 0.5 h / 0 °C

4.2: 78 percent / NaN₃ / hexamethylphosphoric acid triamide / 6 h / 20 °C

With aluminium trichloride; oxalyl dichloride; carbon tetrabromide; dimethyl sulfoxide; triethylamine; triphenylphosphine; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; diethyl ether; dichloromethane; 2.1: Swern oxidation / 3.1: Grignard reaction;
DOI:10.1016/S0968-0896(02)00030-5