4,6-Dichloro-1-<2-deoxy-3,5-bis-O-(4-methylbenzoyl)-β-D-erythro-pentofuranosyl>-1H-pyrrolo<3,2-c>pyridine

Base Information

Chemical Name:4,6-Dichloro-1-<2-deoxy-3,5-bis-O-(4-methylbenzoyl)-β-D-erythro-pentofuranosyl>-1H-pyrrolo<3,2-c>pyridine
CAS No.:91713-48-3
Molecular Formula:C₂₈H₂₄Cl₂N₂O₅
Molecular Weight:539.415
Hs Code.:

Synonyms:4,6-Dichloro-1-<2-deoxy-3,5-bis-O-(4-methylbenzoyl)-β-D-erythro-pentofuranosyl>-1H-pyrrolo<3,2-c>pyridine

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Chemical Property of 4,6-Dichloro-1-<2-deoxy-3,5-bis-O-(4-methylbenzoyl)-β-D-erythro-pentofuranosyl>-1H-pyrrolo<3,2-c>pyridine

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Technology Process of 4,6-Dichloro-1-<2-deoxy-3,5-bis-O-(4-methylbenzoyl)-β-D-erythro-pentofuranosyl>-1H-pyrrolo<3,2-c>pyridine

There total 1 articles about 4,6-Dichloro-1-<2-deoxy-3,5-bis-O-(4-methylbenzoyl)-β-D-erythro-pentofuranosyl>-1H-pyrrolo<3,2-c>pyridine 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: 90.0%

: 4330-21-6
2-deoxy-3,5-di-O-p-toluoyl-α-D-erythro-pentofuranosyl chloride

: 67139-79-1
4,6-dichloro-1H-pyrrolo<3,2-c>pyridine

: 91713-48-3
4,6-Dichloro-1-<2-deoxy-3,5-bis-O-(4-methylbenzoyl)-β-D-erythro-pentofuranosyl>-1H-pyrrolo<3,2-c>pyridine

Guidance literature:: With potassium hydroxide; cryptand TDA-1; In acetonitrile; for 0.75h; Ambient temperature;
DOI:10.1055/s-1988-27759

Reference yield:

: 91713-48-3
4,6-Dichloro-1-<2-deoxy-3,5-bis-O-(4-methylbenzoyl)-β-D-erythro-pentofuranosyl>-1H-pyrrolo<3,2-c>pyridine

: 120552-25-2
4,6-Dichloro-1-(2,3-dideoxy-β-D-glycero-pentofuranosyl)-5'-O-(4,4'-dimethoxytrityl)-1H-pyrrolo<3,2-c>pyridine

Guidance literature:: Multi-step reaction with 4 steps

1: 72 percent / NH₃ / methanol / 12 h / 50 °C

2: 74 percent / ethyldiisopropylamine / pyridine / 1 h / Ambient temperature

3: 84 percent / 4-dimethylaminopyridine / acetonitrile / 16 h / Ambient temperature

4: 85 percent / AIBN, tributylstannane / toluene / 3 h / 80 °C

With dmap; 2,2'-azobis(isobutyronitrile); ammonia; tri-n-butyl-tin hydride; N-ethyl-N,N-diisopropylamine; In pyridine; methanol; toluene; acetonitrile;
DOI:10.1055/s-1988-27759

Reference yield:

: 91713-48-3
4,6-Dichloro-1-<2-deoxy-3,5-bis-O-(4-methylbenzoyl)-β-D-erythro-pentofuranosyl>-1H-pyrrolo<3,2-c>pyridine

: 120552-23-0
4,6-Dichloro-1-(2-deoxy-β-D-erythro-pentofuranosyl)-5'-O-(4,4'-dimethoxytrityl)-1H-pyrrolo<3,2-c>pyridine

Guidance literature:: Multi-step reaction with 2 steps

1: 72 percent / NH₃ / methanol / 12 h / 50 °C

2: 74 percent / ethyldiisopropylamine / pyridine / 1 h / Ambient temperature

With ammonia; N-ethyl-N,N-diisopropylamine; In pyridine; methanol;
DOI:10.1055/s-1988-27759