9-((1R,4R)-4-(tert-butyldiphenylsilyloxy)-7-fluoro-1,2,3,4-tetrahydronaphthalen-1-yl)-2-(6-fluoro-1H-benzo[d]imidazol-1-yl)-7H-purin-8(9H)-one

Base Information

Chemical Name:9-((1R,4R)-4-(tert-butyldiphenylsilyloxy)-7-fluoro-1,2,3,4-tetrahydronaphthalen-1-yl)-2-(6-fluoro-1H-benzo[d]imidazol-1-yl)-7H-purin-8(9H)-one
CAS No.:1083302-77-5
Molecular Formula:C₃₈H₃₄F₂N₆O₂Si
Molecular Weight:672.809
Hs Code.:

Synonyms:9-((1R,4R)-4-(tert-butyldiphenylsilyloxy)-7-fluoro-1,2,3,4-tetrahydronaphthalen-1-yl)-2-(6-fluoro-1H-benzo[d]imidazol-1-yl)-7H-purin-8(9H)-one

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Chemical Property of 9-((1R,4R)-4-(tert-butyldiphenylsilyloxy)-7-fluoro-1,2,3,4-tetrahydronaphthalen-1-yl)-2-(6-fluoro-1H-benzo[d]imidazol-1-yl)-7H-purin-8(9H)-one

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Technology Process of 9-((1R,4R)-4-(tert-butyldiphenylsilyloxy)-7-fluoro-1,2,3,4-tetrahydronaphthalen-1-yl)-2-(6-fluoro-1H-benzo[d]imidazol-1-yl)-7H-purin-8(9H)-one

There total 16 articles about 9-((1R,4R)-4-(tert-butyldiphenylsilyloxy)-7-fluoro-1,2,3,4-tetrahydronaphthalen-1-yl)-2-(6-fluoro-1H-benzo[d]imidazol-1-yl)-7H-purin-8(9H)-one 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: 82.0%

: 1083302-74-2
N₄-((1R,4R)-4-(tert-butyldiphenylsilyloxy)-7-fluoro-1,2,3,4-tetrahydronaphthalen-1-yl)-2-(6-fluoro-1H-benzo[d]imidazol-1-yl)pyrimidine-4,5-diamine

: 530-62-1
1,1'-carbonyldiimidazole

: 1083302-77-5
9-((1R,4R)-4-(tert-butyldiphenylsilyloxy)-7-fluoro-1,2,3,4-tetrahydronaphthalen-1-yl)-2-(6-fluoro-1H-benzo[d]imidazol-1-yl)-7H-purin-8(9H)-one

Guidance literature:: In tetrahydrofuran; at 20 ℃;

Reference yield:

: tert-butyl-N-((tert-butoxy)carbonyl)-N-(4-fluoro-2-nitrophenyl)carbamate

: 1083302-77-5
9-((1R,4R)-4-(tert-butyldiphenylsilyloxy)-7-fluoro-1,2,3,4-tetrahydronaphthalen-1-yl)-2-(6-fluoro-1H-benzo[d]imidazol-1-yl)-7H-purin-8(9H)-one

Guidance literature:: Multi-step reaction with 7 steps

1: trifluoroacetic acid / dichloromethane / 3 h

2: potassium carbonate / acetonitrile / 15 h

3: trifluoroacetic acid / dichloromethane / 1.5 h

4: methanol / 16 h

5: N-ethyl-N,N-diisopropylamine / tetrahydrofuran; dimethyl sulfoxide / 16 h / 20 °C

6: hydrogen / 10percent platinum on carbon, sulfided / methanol; ethyl acetate / 5 h / 2068.65 Torr

7: tetrahydrofuran / 20 °C

With hydrogen; potassium carbonate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; 10percent platinum on carbon, sulfided; In tetrahydrofuran; methanol; dichloromethane; dimethyl sulfoxide; ethyl acetate; acetonitrile;

Reference yield:

: 911826-14-7
tert-butyl 4-fluoro-2-(5-nitro-4-thiocyanatopyrimidin-2-ylamino)phenylcarbamate

: 1083302-77-5
9-((1R,4R)-4-(tert-butyldiphenylsilyloxy)-7-fluoro-1,2,3,4-tetrahydronaphthalen-1-yl)-2-(6-fluoro-1H-benzo[d]imidazol-1-yl)-7H-purin-8(9H)-one

Guidance literature:: Multi-step reaction with 5 steps

1: trifluoroacetic acid / dichloromethane / 1.5 h

2: methanol / 16 h

3: N-ethyl-N,N-diisopropylamine / tetrahydrofuran; dimethyl sulfoxide / 16 h / 20 °C

4: hydrogen / 10percent platinum on carbon, sulfided / methanol; ethyl acetate / 5 h / 2068.65 Torr

5: tetrahydrofuran / 20 °C

With hydrogen; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; 10percent platinum on carbon, sulfided; In tetrahydrofuran; methanol; dichloromethane; dimethyl sulfoxide; ethyl acetate;