5-Dimethylamino-1-isopropyl-4-methyl-4-phenyl-2-(tosylimino)imidazolidin

Base Information

Chemical Name:5-Dimethylamino-1-isopropyl-4-methyl-4-phenyl-2-(tosylimino)imidazolidin
CAS No.:77767-61-4
Molecular Formula:C₂₂H₃₀N₄O₂S
Molecular Weight:414.572
Hs Code.:

Synonyms:5-Dimethylamino-1-isopropyl-4-methyl-4-phenyl-2-(tosylimino)imidazolidin

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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 5-Dimethylamino-1-isopropyl-4-methyl-4-phenyl-2-(tosylimino)imidazolidin

Chemical Property:

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Technology Process of 5-Dimethylamino-1-isopropyl-4-methyl-4-phenyl-2-(tosylimino)imidazolidin

There total 3 articles about 5-Dimethylamino-1-isopropyl-4-methyl-4-phenyl-2-(tosylimino)imidazolidin 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: 86.0%

: 77767-42-1
N-(4-Dimethylimonio-3-isopropyl-5-methyl-5-phenyl-1-imidazolin-2-yl)tosylamidat

: 77767-61-4
5-Dimethylamino-1-isopropyl-4-methyl-4-phenyl-2-(tosylimino)imidazolidin

Guidance literature:: With sodium tetrahydroborate; In acetonitrile;

Reference yield:

: 19978-10-0
Isopropyl(tosyl)carbodiimid

: 77767-61-4
5-Dimethylamino-1-isopropyl-4-methyl-4-phenyl-2-(tosylimino)imidazolidin

Guidance literature:: Multi-step reaction with 2 steps

1: 36 percent / diethyl ether / Ambient temperature

2: 86 percent / NaBH₄ / acetonitrile

With sodium tetrahydroborate; In diethyl ether; acetonitrile;

Reference yield:

: 64276-77-3
3-Dimethylamino-2-methyl-2-phenyl-2H-azirin

: 77767-61-4
5-Dimethylamino-1-isopropyl-4-methyl-4-phenyl-2-(tosylimino)imidazolidin

Guidance literature:: Multi-step reaction with 2 steps

1: 36 percent / diethyl ether / Ambient temperature

2: 86 percent / NaBH₄ / acetonitrile

With sodium tetrahydroborate; In diethyl ether; acetonitrile;