(4S)-2-[(N-benzyl-N-phenyl)aminomethyl]-4-(N-benzyloxycarbonyl-2-aminoethyl)imidazoline

Base Information

Chemical Name:(4S)-2-[(N-benzyl-N-phenyl)aminomethyl]-4-(N-benzyloxycarbonyl-2-aminoethyl)imidazoline
CAS No.:1269604-24-1
Molecular Formula:C₂₇H₃₀N₄O₂
Molecular Weight:442.561
Hs Code.:

Synonyms:(4S)-2-[(N-benzyl-N-phenyl)aminomethyl]-4-(N-benzyloxycarbonyl-2-aminoethyl)imidazoline

Suppliers and Price of (4S)-2-[(N-benzyl-N-phenyl)aminomethyl]-4-(N-benzyloxycarbonyl-2-aminoethyl)imidazoline

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (4S)-2-[(N-benzyl-N-phenyl)aminomethyl]-4-(N-benzyloxycarbonyl-2-aminoethyl)imidazoline

Chemical Property:

Purity/Quality:

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Technology Process of (4S)-2-[(N-benzyl-N-phenyl)aminomethyl]-4-(N-benzyloxycarbonyl-2-aminoethyl)imidazoline

There total 1 articles about (4S)-2-[(N-benzyl-N-phenyl)aminomethyl]-4-(N-benzyloxycarbonyl-2-aminoethyl)imidazoline 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:

: 758640-21-0,103-32-2
N-Benzylaniline

: 1269488-21-2
(4S)-4-(N-benzyloxycarbonyl-2-aminoethyl)-2-(chloromethyl)imidazoline hydrochloride

: 1269604-24-1
(4S)-2-[(N-benzyl-N-phenyl)aminomethyl]-4-(N-benzyloxycarbonyl-2-aminoethyl)imidazoline

Guidance literature:: In ethanol; for 24h; Reflux;
DOI:10.1016/j.bmc.2010.11.039

Reference yield:

: 1269604-24-1
(4S)-2-[(N-benzyl-N-phenyl)aminomethyl]-4-(N-benzyloxycarbonyl-2-aminoethyl)imidazoline

: 1269488-32-5
(4S)-2-[(N-benzyl-N-phenyl)aminomethyl]-4-(N-benzyloxycarbonyl-2-aminoethyl)imidazoline hydrochloride

Guidance literature:: With hydrogenchloride; In methanol;
DOI:10.1016/j.bmc.2010.11.039

Reference yield:

: 1269604-24-1
(4S)-2-[(N-benzyl-N-phenyl)aminomethyl]-4-(N-benzyloxycarbonyl-2-aminoethyl)imidazoline

: (4S)-4-(2-aminoethyl)-2-[(N-benzyl-N-phenyl)aminomethyl]imidazoline trihydrobromide

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / methanol

2: hydrogen bromide; acetic acid / 3 h / 20 °C

With hydrogenchloride; hydrogen bromide; acetic acid; In methanol;
DOI:10.1016/j.bmc.2010.11.039