4-((1R,2S)-2-methylcyclohexylamino)-6-nitropyrrolo[1,2-b]pyridazine-3-carboxamide

Base Information

Chemical Name:4-((1R,2S)-2-methylcyclohexylamino)-6-nitropyrrolo[1,2-b]pyridazine-3-carboxamide
CAS No.:1263419-23-3
Molecular Formula:C₁₅H₁₉N₅O₃
Molecular Weight:317.348
Hs Code.:

Synonyms:4-((1R,2S)-2-methylcyclohexylamino)-6-nitropyrrolo[1,2-b]pyridazine-3-carboxamide

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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 4-((1R,2S)-2-methylcyclohexylamino)-6-nitropyrrolo[1,2-b]pyridazine-3-carboxamide

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Technology Process of 4-((1R,2S)-2-methylcyclohexylamino)-6-nitropyrrolo[1,2-b]pyridazine-3-carboxamide

There total 11 articles about 4-((1R,2S)-2-methylcyclohexylamino)-6-nitropyrrolo[1,2-b]pyridazine-3-carboxamide 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: 66.0%

: 1263419-22-2
4-((1R,2S)-2-methylcyclohexylamino)-6-nitropyrrolo[1,2-b]pyridazine-3-carbonitrile

: 1263419-23-3
4-((1R,2S)-2-methylcyclohexylamino)-6-nitropyrrolo[1,2-b]pyridazine-3-carboxamide

Guidance literature:: With ammonium hydroxide; dihydrogen peroxide; In ethanol; water; at 20 ℃; for 16h;

Reference yield:

: 583-60-8
2-Methylcyclohexanone

: 1263419-23-3
4-((1R,2S)-2-methylcyclohexylamino)-6-nitropyrrolo[1,2-b]pyridazine-3-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1: toluene-4-sulfonic acid / benzene / 72 h / Reflux

2: hydrogen / ethanol / 24 h / 3102.97 Torr

3: hydrogen / palladium 10% on activated carbon / ethanol / 24 h / 2585.81 Torr

4: triethylamine / N,N-dimethyl-formamide / 20 °C

5: ammonium hydroxide; dihydrogen peroxide / ethanol; water / 16 h / 20 °C

With ammonium hydroxide; hydrogen; dihydrogen peroxide; toluene-4-sulfonic acid; triethylamine; palladium 10% on activated carbon; In ethanol; water; N,N-dimethyl-formamide; benzene;

Reference yield:

: 73739-21-6,73739-26-1,76947-33-6,91603-24-6,91603-47-3,91603-48-4,91603-49-5,91603-50-8,91603-51-9,91603-52-0,92761-49-4,125515-62-0,125515-69-7,125515-72-2,125515-73-3
(R,Z)-N-(2-methylcyclohexylidene)-1-phenylethaneamine

: 1263419-23-3
4-((1R,2S)-2-methylcyclohexylamino)-6-nitropyrrolo[1,2-b]pyridazine-3-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogen / ethanol / 24 h / 3102.97 Torr

2: hydrogen / palladium 10% on activated carbon / ethanol / 24 h / 2585.81 Torr

3: triethylamine / N,N-dimethyl-formamide / 20 °C

4: ammonium hydroxide; dihydrogen peroxide / ethanol; water / 16 h / 20 °C

With ammonium hydroxide; hydrogen; dihydrogen peroxide; triethylamine; palladium 10% on activated carbon; In ethanol; water; N,N-dimethyl-formamide;