(3R)-6,7-bis(hydroxymethyl)-3-(4-hydroxyphenyl)-5-methyl-1H,3H-pyrrolo[1,2-c]thiazole

Base Information

Chemical Name:(3R)-6,7-bis(hydroxymethyl)-3-(4-hydroxyphenyl)-5-methyl-1H,3H-pyrrolo[1,2-c]thiazole
CAS No.:1609535-73-0
Molecular Formula:C₁₅H₁₇NO₃S
Molecular Weight:291.371
Hs Code.:

Synonyms:(3R)-6,7-bis(hydroxymethyl)-3-(4-hydroxyphenyl)-5-methyl-1H,3H-pyrrolo[1,2-c]thiazole

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Chemical Property of (3R)-6,7-bis(hydroxymethyl)-3-(4-hydroxyphenyl)-5-methyl-1H,3H-pyrrolo[1,2-c]thiazole

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Technology Process of (3R)-6,7-bis(hydroxymethyl)-3-(4-hydroxyphenyl)-5-methyl-1H,3H-pyrrolo[1,2-c]thiazole

There total 3 articles about (3R)-6,7-bis(hydroxymethyl)-3-(4-hydroxyphenyl)-5-methyl-1H,3H-pyrrolo[1,2-c]thiazole 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: 52.0%

: 1609535-72-9
dimethyl (3R)-3-(4-acethoxyphenyl)-5-methyl-1H,3H-pyrrolo[1,2-c]thiazole-6,7-dicarboxylate

: 1609535-73-0
(3R)-6,7-bis(hydroxymethyl)-3-(4-hydroxyphenyl)-5-methyl-1H,3H-pyrrolo[1,2-c]thiazole

Guidance literature:: dimethyl (3R)-3-(4-acethoxyphenyl)-5-methyl-1H,3H-pyrrolo[1,2-c]thiazole-6,7-dicarboxylate; With lithium aluminium tetrahydride; In diethyl ether; dichloromethane; at 0 ℃;

In dichloromethane; di-isopropyl ether; for 1.5h; Reflux;
DOI:10.1016/j.ejmech.2014.04.008

Reference yield:

: 222404-24-2,69588-11-0
(2RS,4R)-2-(4-hydroxyphenyl)-1,3-thiazolidine-4-carboxylic acid

: 1609535-73-0
(3R)-6,7-bis(hydroxymethyl)-3-(4-hydroxyphenyl)-5-methyl-1H,3H-pyrrolo[1,2-c]thiazole

Guidance literature:: Multi-step reaction with 2 steps

1.1: acetic anhydride / 4 h / 110 °C

2.1: lithium aluminium tetrahydride / diethyl ether; dichloromethane / 0 °C

2.2: 1.5 h / Reflux

With lithium aluminium tetrahydride; acetic anhydride; In diethyl ether; dichloromethane;
DOI:10.1016/j.ejmech.2014.04.008

Reference yield:

: 123-08-0,65581-83-1
4-hydroxy-benzaldehyde

: 1609535-73-0
(3R)-6,7-bis(hydroxymethyl)-3-(4-hydroxyphenyl)-5-methyl-1H,3H-pyrrolo[1,2-c]thiazole

Guidance literature:: Multi-step reaction with 3 steps

1.1: water / 20 °C

2.1: acetic anhydride / 4 h / 110 °C

3.1: lithium aluminium tetrahydride / diethyl ether; dichloromethane / 0 °C

3.2: 1.5 h / Reflux

With lithium aluminium tetrahydride; acetic anhydride; In diethyl ether; dichloromethane; water;
DOI:10.1016/j.ejmech.2014.04.008