N-[(1R)-6-[(tert-butylamino)methyl]-1,2,3,4-tetrahydronaphthalen-1-yl]-2-[2-(p-tolylsulfonyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-1-yl]acetamide

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Chemical Name:N-[(1R)-6-[(tert-butylamino)methyl]-1,2,3,4-tetrahydronaphthalen-1-yl]-2-[2-(p-tolylsulfonyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-1-yl]acetamide
CAS No.:1242847-70-6
Molecular Formula:C₃₁H₄₀N₄O₃S
Molecular Weight:548.75
Hs Code.:

Synonyms:N-[(1R)-6-[(tert-butylamino)methyl]-1,2,3,4-tetrahydronaphthalen-1-yl]-2-[2-(p-tolylsulfonyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-1-yl]acetamide

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Chemical Property of N-[(1R)-6-[(tert-butylamino)methyl]-1,2,3,4-tetrahydronaphthalen-1-yl]-2-[2-(p-tolylsulfonyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-1-yl]acetamide

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Technology Process of N-[(1R)-6-[(tert-butylamino)methyl]-1,2,3,4-tetrahydronaphthalen-1-yl]-2-[2-(p-tolylsulfonyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-1-yl]acetamide

There total 8 articles about N-[(1R)-6-[(tert-butylamino)methyl]-1,2,3,4-tetrahydronaphthalen-1-yl]-2-[2-(p-tolylsulfonyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-1-yl]acetamide 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: 19.0%

: (R)-6-((tert-butylamino)methyl)-1,2,3,4-tetrahydronaphthalen-1-ylamine

: 1242850-08-3
2-(2-tosyl-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-1-yl)acetic acid

: 1242847-70-6
N-[(1R)-6-[(tert-butylamino)methyl]-1,2,3,4-tetrahydronaphthalen-1-yl]-2-[2-(p-tolylsulfonyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-1-yl]acetamide

Guidance literature:: 2-(2-tosyl-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-1-yl)acetic acid; With N-ethyl-N,N-diisopropylamine; HATU; In tetrahydrofuran; at 0 ℃; for 0.25h;

(R)-6-((tert-butylamino)methyl)-1,2,3,4-tetrahydronaphthalen-1-ylamine; In tetrahydrofuran; at 20 ℃; for 16h;

Reference yield:

: 828925-93-5
methyl 5-(R)-azido-5,6,7,8-tetrahydronaphthalene-2-carboxylate

: 1242847-70-6
N-[(1R)-6-[(tert-butylamino)methyl]-1,2,3,4-tetrahydronaphthalen-1-yl]-2-[2-(p-tolylsulfonyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-1-yl]acetamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: lithium aluminium tetrahydride / tetrahydrofuran / 25 °C / Cooling

2.1: dichloromethane / 0 - 20 °C

3.1: triethylamine / dichloromethane / 0 - 20 °C

4.1: potassium carbonate / tetrahydrofuran / 16 h / Reflux

5.1: trifluoroacetic acid / dichloromethane / 0 - 25 °C

6.1: N-ethyl-N,N-diisopropylamine; HATU / tetrahydrofuran / 0.25 h / 0 °C

6.2: 16 h / 20 °C

With lithium aluminium tetrahydride; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; trifluoroacetic acid; In tetrahydrofuran; dichloromethane;

Reference yield:

: 828914-11-0
(R)-(5-amino-5,6,7,8-tetrahydronaphthalene-2-yl)methanol

: 1242847-70-6
N-[(1R)-6-[(tert-butylamino)methyl]-1,2,3,4-tetrahydronaphthalen-1-yl]-2-[2-(p-tolylsulfonyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-1-yl]acetamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: dichloromethane / 0 - 20 °C

2.1: triethylamine / dichloromethane / 0 - 20 °C

3.1: potassium carbonate / tetrahydrofuran / 16 h / Reflux

4.1: trifluoroacetic acid / dichloromethane / 0 - 25 °C

5.1: N-ethyl-N,N-diisopropylamine; HATU / tetrahydrofuran / 0.25 h / 0 °C

5.2: 16 h / 20 °C

With potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; trifluoroacetic acid; In tetrahydrofuran; dichloromethane;