N-(anilinocarbonyl)amino(diethylamino)methylidene-2,2-dimethylpropanamide

Base Information

Chemical Name:N-(anilinocarbonyl)amino(diethylamino)methylidene-2,2-dimethylpropanamide
CAS No.:371779-15-6
Molecular Formula:C₁₇H₂₆N₄O₂
Molecular Weight:318.419
Hs Code.:

Synonyms:N-(anilinocarbonyl)amino(diethylamino)methylidene-2,2-dimethylpropanamide

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Chemical Property of N-(anilinocarbonyl)amino(diethylamino)methylidene-2,2-dimethylpropanamide

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Technology Process of N-(anilinocarbonyl)amino(diethylamino)methylidene-2,2-dimethylpropanamide

There total 3 articles about N-(anilinocarbonyl)amino(diethylamino)methylidene-2,2-dimethylpropanamide 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: 89.0%

: 64-10-8
phenyl carbamate

: N-[1H-Benzotriazol-1-yl(diethylamino)methylidene]-2,2-dimethylpropanamide

: 371779-15-6
N-(anilinocarbonyl)amino(diethylamino)methylidene-2,2-dimethylpropanamide

Guidance literature:: With potassium tert-butylate; In tetrahydrofuran; at 20 ℃;
DOI:10.1021/jo010416a

Reference yield:

: 3282-30-2
pivaloyl chloride

: 371779-15-6
N-(anilinocarbonyl)amino(diethylamino)methylidene-2,2-dimethylpropanamide

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / triethylamine / CHCl₃ / 20 °C

2: 89 percent / potassium tert-butoxide / tetrahydrofuran / 20 °C

With potassium tert-butylate; triethylamine; In tetrahydrofuran; chloroform;
DOI:10.1021/jo010416a

Reference yield:

: 351425-47-3
N,N-Diethyl-1H-benzotriazole-1-carboximidamide

: 371779-15-6
N-(anilinocarbonyl)amino(diethylamino)methylidene-2,2-dimethylpropanamide

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / triethylamine / CHCl₃ / 20 °C

2: 89 percent / potassium tert-butoxide / tetrahydrofuran / 20 °C

With potassium tert-butylate; triethylamine; In tetrahydrofuran; chloroform;
DOI:10.1021/jo010416a