C₂₅H₂₃N₇O₃S

Base Information

Chemical Name:C₂₅H₂₃N₇O₃S
CAS No.:1125635-16-6
Molecular Formula:C₂₅H₂₃N₇O₃S
Molecular Weight:501.569
Hs Code.:

C<sub>25</sub>H<sub>23</sub>N<sub>7</sub>O<sub>3</sub>S

Synonyms:C₂₅H₂₃N₇O₃S

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Chemical Property of C₂₅H₂₃N₇O₃S

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Technology Process of C₂₅H₂₃N₇O₃S

There total 6 articles about C₂₅H₂₃N₇O₃S 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: 46.0%

: 1123582-40-0
3-(1-cyano-1-methylethoxy)benzoic acid

: 1125633-22-8
N-{5-[(5-amino-2-methylphenyl)amino][1,3]thiazolo[5,4-d]pyrimidin-2-yl}acetamide

: 1125635-16-6
C₂₅H₂₃N₇O₃S

Guidance literature:: With pyridine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; at 20 ℃; for 1h;
DOI:10.1016/j.bmc.2012.07.032

Reference yield:

: 1123582-38-6
methyl 3-(1-cyano-1-methylethoxy)benzoate

: 1125635-16-6
C₂₅H₂₃N₇O₃S

Guidance literature:: Multi-step reaction with 2 steps

1: methanol; sodium hydroxide / tetrahydrofuran / 4 h / 60 °C

2: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; pyridine / 1 h / 20 °C

With pyridine; methanol; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; sodium hydroxide; In tetrahydrofuran;
DOI:10.1016/j.bmc.2012.07.032

Reference yield:

: 119-32-4
4-Methyl-3-nitroanilin

: 1125635-16-6
C₂₅H₂₃N₇O₃S

Guidance literature:: Multi-step reaction with 7 steps

1: tetrahydrofuran / 15.5 h / 70 °C

2: 10% Pd/C; hydrogen / tetrahydrofuran; ethanol / 22 h / 20 °C / 2280.15 Torr

3: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 0.5 h / 10 - 20 °C

4: iron; calcium chloride / ethanol; water; 1-methyl-pyrrolidin-2-one / 16 h / 100 °C

5: pyridine / 1 h / 0 - 20 °C

6: methoxybenzene; trifluoroacetic acid / 1 h / 0 °C

7: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; pyridine / 1 h / 20 °C

With pyridine; 10% Pd/C; hydrogen; iron; methoxybenzene; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; calcium chloride; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; ethanol; water;
DOI:10.1016/j.bmc.2012.07.032