ethyl 4-<(2-(pivaloylamino)-6-methyl-3,4-dihydro-4-oxo-7H-pyrrolo<2,3-d>pyrimidin-5-yl)sulfanyl>benzoate

Base Information

Chemical Name:ethyl 4-<(2-(pivaloylamino)-6-methyl-3,4-dihydro-4-oxo-7H-pyrrolo<2,3-d>pyrimidin-5-yl)sulfanyl>benzoate
CAS No.:172287-81-9
Molecular Formula:C₂₁H₂₄N₄O₄S
Molecular Weight:428.512
Hs Code.:

Synonyms:ethyl 4-<(2-(pivaloylamino)-6-methyl-3,4-dihydro-4-oxo-7H-pyrrolo<2,3-d>pyrimidin-5-yl)sulfanyl>benzoate

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Chemical Property of ethyl 4-<(2-(pivaloylamino)-6-methyl-3,4-dihydro-4-oxo-7H-pyrrolo<2,3-d>pyrimidin-5-yl)sulfanyl>benzoate

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Technology Process of ethyl 4-<(2-(pivaloylamino)-6-methyl-3,4-dihydro-4-oxo-7H-pyrrolo<2,3-d>pyrimidin-5-yl)sulfanyl>benzoate

There total 4 articles about ethyl 4-<(2-(pivaloylamino)-6-methyl-3,4-dihydro-4-oxo-7H-pyrrolo<2,3-d>pyrimidin-5-yl)sulfanyl>benzoate 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: 36.0%

: sodium salt of ethyl 4-mercaptobenzoate

: 172287-76-2
2-(pivaloylamino)-6-methyl-3,4-dihydro-4-oxo-7H-pyrrolo<2,3-d>pyrimidine

: 172287-82-0
ethyl 4-<(2-amino-6-methyl-3,4-dihydro-4-oxo-7H-pyrrolo<2,3-d>pyrimidin-5-yl)sulfanyl>benzoate

: 172287-81-9
ethyl 4-<(2-(pivaloylamino)-6-methyl-3,4-dihydro-4-oxo-7H-pyrrolo<2,3-d>pyrimidin-5-yl)sulfanyl>benzoate

Guidance literature:: With iodine; In ethanol; water; 1.) 80 deg C, 2.) reflux, 1.5 h;
DOI:10.1021/jm00022a015

Reference yield:

: 1155-51-7
4,4'-Dithiobisbenzoic acid

: 172287-81-9
ethyl 4-<(2-(pivaloylamino)-6-methyl-3,4-dihydro-4-oxo-7H-pyrrolo<2,3-d>pyrimidin-5-yl)sulfanyl>benzoate

Guidance literature:: Multi-step reaction with 3 steps

1: 81 percent / sodium bicarbonate / N,N-dimethyl-acetamide / 120 h

2: sodium borohydride / ethanol / 0.5 h

3: 36 percent / iodine / ethanol; H₂O / 1.) 80 deg C, 2.) reflux, 1.5 h

With sodium tetrahydroborate; iodine; sodium hydrogencarbonate; In ethanol; N,N-dimethyl acetamide; water;
DOI:10.1021/jm00022a015

Reference yield:

: 20057-83-4
diethyl 4,4'-dithiobis

: 172287-81-9
ethyl 4-<(2-(pivaloylamino)-6-methyl-3,4-dihydro-4-oxo-7H-pyrrolo<2,3-d>pyrimidin-5-yl)sulfanyl>benzoate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium borohydride / ethanol / 0.5 h

2: 36 percent / iodine / ethanol; H₂O / 1.) 80 deg C, 2.) reflux, 1.5 h

With sodium tetrahydroborate; iodine; In ethanol; water;
DOI:10.1021/jm00022a015