(S)-N-((R)-(4-(benzyloxy)phenyl)((R)-pyrrolidin-2-yl)methyl)-2-phenylpropanamide

Base Information

Chemical Name:(S)-N-((R)-(4-(benzyloxy)phenyl)((R)-pyrrolidin-2-yl)methyl)-2-phenylpropanamide
CAS No.:1287286-79-6
Molecular Formula:C₂₇H₃₀N₂O₂
Molecular Weight:414.547
Hs Code.:

Synonyms:(S)-N-((R)-(4-(benzyloxy)phenyl)((R)-pyrrolidin-2-yl)methyl)-2-phenylpropanamide

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Chemical Property of (S)-N-((R)-(4-(benzyloxy)phenyl)((R)-pyrrolidin-2-yl)methyl)-2-phenylpropanamide

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Technology Process of (S)-N-((R)-(4-(benzyloxy)phenyl)((R)-pyrrolidin-2-yl)methyl)-2-phenylpropanamide

There total 5 articles about (S)-N-((R)-(4-(benzyloxy)phenyl)((R)-pyrrolidin-2-yl)methyl)-2-phenylpropanamide 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: 61.9%

: 1287286-77-4
(R)-tert-butyl 2-((R)-(4-(benzyloxy)phenyl)((S)-2-phenylpropanamido)methyl)pyrrolidine-1-carboxylate

: 1287286-79-6
(S)-N-((R)-(4-(benzyloxy)phenyl)((R)-pyrrolidin-2-yl)methyl)-2-phenylpropanamide

Guidance literature:: With hydrogenchloride; In diethyl ether; at 20 ℃; for 4h;

Reference yield:

: 288086-98-6
[tert-butyl (R)-2-(methoxy(methyl)carbamoyl)pyrrolidine-1-carboxylate]

: 1287286-79-6
(S)-N-((R)-(4-(benzyloxy)phenyl)((R)-pyrrolidin-2-yl)methyl)-2-phenylpropanamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: tetrahydrofuran / 0 - 65 °C

1.2: 0 °C

2.1: ammonium acetate / methanol / 0.5 h / 20 °C

2.2: 72 h / 60 °C

3.1: dicyclohexyl-carbodiimide; N-ethyl-N,N-diisopropylamine; benzotriazol-1-ol / dichloromethane / 0.17 h / 20 °C

3.2: 4 h / 20 °C

4.1: hydrogenchloride / diethyl ether / 4 h / 20 °C

With hydrogenchloride; ammonium acetate; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; diethyl ether; dichloromethane;

Reference yield:

: 37784-17-1,59433-50-0
N-(tert-butoxycarbonyl)-D-proline

: 1287286-79-6
(S)-N-((R)-(4-(benzyloxy)phenyl)((R)-pyrrolidin-2-yl)methyl)-2-phenylpropanamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: dicyclohexyl-carbodiimide; N-ethyl-N,N-diisopropylamine; benzotriazol-1-ol / dichloromethane / 1 h / 20 °C

1.2: 4 h / 20 °C

2.1: tetrahydrofuran / 0 - 65 °C

2.2: 0 °C

3.1: ammonium acetate / methanol / 0.5 h / 20 °C

3.2: 72 h / 60 °C

4.1: dicyclohexyl-carbodiimide; N-ethyl-N,N-diisopropylamine; benzotriazol-1-ol / dichloromethane / 0.17 h / 20 °C

4.2: 4 h / 20 °C

5.1: hydrogenchloride / diethyl ether / 4 h / 20 °C

With hydrogenchloride; ammonium acetate; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; diethyl ether; dichloromethane;