3-formyl-2,5,6-trichloro-1-[3,5-di-(O-p-toluoyl)-2-deoxy-β-D-ribofuranosyl]indole

Base Information

Chemical Name:3-formyl-2,5,6-trichloro-1-[3,5-di-(O-p-toluoyl)-2-deoxy-β-D-ribofuranosyl]indole
CAS No.:800400-51-5
Molecular Formula:C₃₀H₂₄Cl₃NO₆
Molecular Weight:600.883
Hs Code.:

Synonyms:3-formyl-2,5,6-trichloro-1-[3,5-di-(O-p-toluoyl)-2-deoxy-β-D-ribofuranosyl]indole

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Chemical Property of 3-formyl-2,5,6-trichloro-1-[3,5-di-(O-p-toluoyl)-2-deoxy-β-D-ribofuranosyl]indole

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Technology Process of 3-formyl-2,5,6-trichloro-1-[3,5-di-(O-p-toluoyl)-2-deoxy-β-D-ribofuranosyl]indole

There total 2 articles about 3-formyl-2,5,6-trichloro-1-[3,5-di-(O-p-toluoyl)-2-deoxy-β-D-ribofuranosyl]indole 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: 49.0%

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

: 800400-47-9
3-formyl-2,5,6-trichloroindole

: 800400-51-5
3-formyl-2,5,6-trichloro-1-[3,5-di-(O-p-toluoyl)-2-deoxy-β-D-ribofuranosyl]indole

Guidance literature:: 3-formyl-2,5,6-trichloroindole; With sodium hydride; In tetrahydrofuran; at 20 - 25 ℃; for 0.25h;

2-deoxy-3,5-di-O-p-toluoyl-α-D-erythro-pentofuranosyl chloride; In tetrahydrofuran; toluene; at 20 ℃; for 16h;
DOI:10.1021/jm0400606

Reference yield:

: 286949-65-3
2,5,6-trichloroindole

: 800400-51-5
3-formyl-2,5,6-trichloro-1-[3,5-di-(O-p-toluoyl)-2-deoxy-β-D-ribofuranosyl]indole

Guidance literature:: Multi-step reaction with 2 steps

1.1: 73 percent / POCl₃ / 16 h / 60 °C

2.1: NaH / tetrahydrofuran / 0.25 h / 20 - 25 °C

2.2: 49 percent / tetrahydrofuran; toluene / 16 h / 20 °C

With sodium hydride; trichlorophosphate; In tetrahydrofuran; 1.1: Vilesmeier-Haack formylation;
DOI:10.1021/jm0400606