4-Acetylamino-N-((1R,3S,5S)-8-benzyl-8-aza-bicyclo[3.2.1]oct-3-yl)-2-methoxy-benzamide

Base Information

Chemical Name:4-Acetylamino-N-((1R,3S,5S)-8-benzyl-8-aza-bicyclo[3.2.1]oct-3-yl)-2-methoxy-benzamide
CAS No.:84923-55-7
Molecular Formula:C₂₄H₂₉N₃O₃
Molecular Weight:407.513
Hs Code.:

Synonyms:4-Acetylamino-N-((1R,3S,5S)-8-benzyl-8-aza-bicyclo[3.2.1]oct-3-yl)-2-methoxy-benzamide

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Chemical Property of 4-Acetylamino-N-((1R,3S,5S)-8-benzyl-8-aza-bicyclo[3.2.1]oct-3-yl)-2-methoxy-benzamide

Chemical Property:

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Technology Process of 4-Acetylamino-N-((1R,3S,5S)-8-benzyl-8-aza-bicyclo[3.2.1]oct-3-yl)-2-methoxy-benzamide

There total 1 articles about 4-Acetylamino-N-((1R,3S,5S)-8-benzyl-8-aza-bicyclo[3.2.1]oct-3-yl)-2-methoxy-benzamide 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:

: 55304-05-7
4-acetylamino-2-methoxy-benzoic acid

: 84923-55-7
4-Acetylamino-N-((1R,3S,5S)-8-benzyl-8-aza-bicyclo[3.2.1]oct-3-yl)-2-methoxy-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / tetrahydrofuran / 1.5 h / 20 °C

2: tetrahydrofuran / 60 h / 20 °C

With triethylamine; In tetrahydrofuran;
DOI:10.1248/cpb.49.424

Reference yield:

: 84923-55-7
4-Acetylamino-N-((1R,3S,5S)-8-benzyl-8-aza-bicyclo[3.2.1]oct-3-yl)-2-methoxy-benzamide

: 145726-42-7
4-Acetylamino-N-(1S,3S,5R)-8-aza-bicyclo[3.2.1]oct-3-yl-2-methoxy-benzamide

Guidance literature:: With hydrogen; acetic acid; palladium dihydroxide; In methanol; at 20 ℃; for 1h;
DOI:10.1248/cpb.49.424

Reference yield:

: 84923-55-7
4-Acetylamino-N-((1R,3S,5S)-8-benzyl-8-aza-bicyclo[3.2.1]oct-3-yl)-2-methoxy-benzamide

: [(1R,3S,5S)-3-(4-Amino-5-chloro-2-methoxy-benzoylamino)-8-aza-bicyclo[3.2.1]oct-8-yl]-acetic acid

Guidance literature:: Multi-step reaction with 5 steps

1: H₂; acetic acid / 20 percent Pd(OH)2/C / methanol / 1 h / 20 °C

2: K₂CO₃ / dimethylformamide / 2 h / 60 °C

3: SO₂Cl₂ / CH₂Cl₂ / 1.5 h / 20 °C

4: hydrochloride / ethanol / 1 h / Heating

5: 2 N aq. NaOH / methanol / 1 h / Heating

With hydrogenchloride; sodium hydroxide; sulfuryl dichloride; hydrogen; potassium carbonate; acetic acid; palladium dihydroxide; In methanol; ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1248/cpb.49.424