N-benzyl-N-(1-{[(2,2-dimethoxyethyl)amino]carbonothioyl}-2-methylpropyl)acetamide

Base Information

Chemical Name:N-benzyl-N-(1-{[(2,2-dimethoxyethyl)amino]carbonothioyl}-2-methylpropyl)acetamide
CAS No.:866784-78-3
Molecular Formula:C₁₈H₂₈N₂O₃S
Molecular Weight:352.498
Hs Code.:

Synonyms:N-benzyl-N-(1-{[(2,2-dimethoxyethyl)amino]carbonothioyl}-2-methylpropyl)acetamide

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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 N-benzyl-N-(1-{[(2,2-dimethoxyethyl)amino]carbonothioyl}-2-methylpropyl)acetamide

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Technology Process of N-benzyl-N-(1-{[(2,2-dimethoxyethyl)amino]carbonothioyl}-2-methylpropyl)acetamide

There total 4 articles about N-benzyl-N-(1-{[(2,2-dimethoxyethyl)amino]carbonothioyl}-2-methylpropyl)acetamide 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: 75.0%

: 78-84-2
isobutyraldehyde

: 100-46-9
benzylamine

: 507-09-5
tiolacetic acid

: 277300-82-0
isocyanoacetaldehyde dimethylacetale

: 866784-78-3
N-benzyl-N-(1-{[(2,2-dimethoxyethyl)amino]carbonothioyl}-2-methylpropyl)acetamide

Guidance literature:: isobutyraldehyde; benzylamine; In methanol; at 20 ℃; for 0.25h;

tiolacetic acid; isocyanoacetaldehyde dimethylacetale; In methanol; at 20 ℃; Further stages.;
DOI:10.1021/jo071030o

Reference yield:

: 135393-73-6
(N-formylamino)acetaldehyde dimethyl acetal

: 866784-78-3
N-benzyl-N-(1-{[(2,2-dimethoxyethyl)amino]carbonothioyl}-2-methylpropyl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: 57 percent / Et₃N; POCl₃ / CH₂Cl₂ / 1 h / 20 °C

2: methanol / 20 °C

With triethylamine; trichlorophosphate; In methanol; dichloromethane; 2: Ugi reaction;
DOI:10.1039/b507028g