(S)-2-{4-[4-(2-Amino-6-hydroxy-5-nitro-pyrimidin-4-ylamino)-3-oxo-butylsulfanyl]-benzoylamino}-pentanedioic acid diethyl ester

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Chemical Name:(S)-2-{4-[4-(2-Amino-6-hydroxy-5-nitro-pyrimidin-4-ylamino)-3-oxo-butylsulfanyl]-benzoylamino}-pentanedioic acid diethyl ester
CAS No.:74163-09-0
Molecular Formula:C₂₄H₃₀N₆O₉S
Molecular Weight:578.603
Hs Code.:

Synonyms:(S)-2-{4-[4-(2-Amino-6-hydroxy-5-nitro-pyrimidin-4-ylamino)-3-oxo-butylsulfanyl]-benzoylamino}-pentanedioic acid diethyl ester

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Chemical Property of (S)-2-{4-[4-(2-Amino-6-hydroxy-5-nitro-pyrimidin-4-ylamino)-3-oxo-butylsulfanyl]-benzoylamino}-pentanedioic acid diethyl ester

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Technology Process of (S)-2-{4-[4-(2-Amino-6-hydroxy-5-nitro-pyrimidin-4-ylamino)-3-oxo-butylsulfanyl]-benzoylamino}-pentanedioic acid diethyl ester

There total 8 articles about (S)-2-{4-[4-(2-Amino-6-hydroxy-5-nitro-pyrimidin-4-ylamino)-3-oxo-butylsulfanyl]-benzoylamino}-pentanedioic acid diethyl ester 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:

: 67426-03-3
1-chloro-4--2-butanone

: 74163-09-0
(S)-2-{4-[4-(2-Amino-6-hydroxy-5-nitro-pyrimidin-4-ylamino)-3-oxo-butylsulfanyl]-benzoylamino}-pentanedioic acid diethyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: 91 percent / sodium azide, potassium iodide / acetone

2: 85 percent / p-toluenesulfonic acid / benzene / 6 h / Heating

3: 99 percent / 0.5 N aq. NaOH / acetonitrile / 6 h

4: N-methylmorpholine / 0.33 h

5: N-methylmorpholine / dimethylformamide / 18 h

6: H₂ / 5percent Pd/C

7: N-methylmorpholine / methanol / 4 h / Heating

8: trifluoroacetic acid (TFA) / 0.5 h / 50 °C

With 4-methyl-morpholine; sodium hydroxide; sodium azide; hydrogen; toluene-4-sulfonic acid; trifluoroacetic acid; potassium iodide; palladium on activated charcoal; In methanol; N,N-dimethyl-formamide; acetone; acetonitrile; benzene;
DOI:10.1021/jm00182a017

Reference yield:

: 74162-96-2
1-azido-4--2-butanone

: 74163-09-0
(S)-2-{4-[4-(2-Amino-6-hydroxy-5-nitro-pyrimidin-4-ylamino)-3-oxo-butylsulfanyl]-benzoylamino}-pentanedioic acid diethyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 85 percent / p-toluenesulfonic acid / benzene / 6 h / Heating

2: 99 percent / 0.5 N aq. NaOH / acetonitrile / 6 h

3: N-methylmorpholine / 0.33 h

4: N-methylmorpholine / dimethylformamide / 18 h

5: H₂ / 5percent Pd/C

6: N-methylmorpholine / methanol / 4 h / Heating

7: trifluoroacetic acid (TFA) / 0.5 h / 50 °C

With 4-methyl-morpholine; sodium hydroxide; hydrogen; toluene-4-sulfonic acid; trifluoroacetic acid; palladium on activated charcoal; In methanol; N,N-dimethyl-formamide; acetonitrile; benzene;
DOI:10.1021/jm00182a017

Reference yield:

: 74162-98-4
4-[2-(2-Azidomethyl-[1,3]dioxolan-2-yl)-ethylsulfanyl]-benzoic acid

: 74163-09-0
(S)-2-{4-[4-(2-Amino-6-hydroxy-5-nitro-pyrimidin-4-ylamino)-3-oxo-butylsulfanyl]-benzoylamino}-pentanedioic acid diethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: N-methylmorpholine / 0.33 h

2: N-methylmorpholine / dimethylformamide / 18 h

3: H₂ / 5percent Pd/C

4: N-methylmorpholine / methanol / 4 h / Heating

5: trifluoroacetic acid (TFA) / 0.5 h / 50 °C

With 4-methyl-morpholine; hydrogen; trifluoroacetic acid; palladium on activated charcoal; In methanol; N,N-dimethyl-formamide;
DOI:10.1021/jm00182a017