(R)-4-[6-Benzyloxy-1-(morpholine-4-carbonyl)-1H-indole-3-carbonyl]-2-pyridin-3-yl-thiazolidine-3-carboxylic acid tert-butyl ester

Base Information

Chemical Name:(R)-4-[6-Benzyloxy-1-(morpholine-4-carbonyl)-1H-indole-3-carbonyl]-2-pyridin-3-yl-thiazolidine-3-carboxylic acid tert-butyl ester
CAS No.:1027527-06-5
Molecular Formula:C₃₄H₃₆N₄O₆S
Molecular Weight:628.749
Hs Code.:

Synonyms:(R)-4-[6-Benzyloxy-1-(morpholine-4-carbonyl)-1H-indole-3-carbonyl]-2-pyridin-3-yl-thiazolidine-3-carboxylic acid tert-butyl ester

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Chemical Property of (R)-4-[6-Benzyloxy-1-(morpholine-4-carbonyl)-1H-indole-3-carbonyl]-2-pyridin-3-yl-thiazolidine-3-carboxylic acid tert-butyl ester

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Technology Process of (R)-4-[6-Benzyloxy-1-(morpholine-4-carbonyl)-1H-indole-3-carbonyl]-2-pyridin-3-yl-thiazolidine-3-carboxylic acid tert-butyl ester

There total 5 articles about (R)-4-[6-Benzyloxy-1-(morpholine-4-carbonyl)-1H-indole-3-carbonyl]-2-pyridin-3-yl-thiazolidine-3-carboxylic acid tert-butyl ester 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:

: 500-22-1
3-pyridinecarboxaldehyde

: 1027527-06-5
(R)-4-[6-Benzyloxy-1-(morpholine-4-carbonyl)-1H-indole-3-carbonyl]-2-pyridin-3-yl-thiazolidine-3-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 81 percent / ethanol; H₂O / 5 h / 100 °C

2: 80 percent / NaOH / dioxane / 19 h

3: 1.) NaH, 2.) oxalyl chloride / 1.) CH₂Cl₂, until gas evolution ceased, 2.) CH₂Cl₂, RT, 30 min

4: 1.) ethylmagnesium chloride / 1.) benzene, ether, 20 min, 2.) benzene, ether, CH₂Cl₂, RT, 3 h

5: 1.) KOH / 1.) DME, 0 deg C, 10 min, 2.) DME, RT, 30 min

With potassium hydroxide; sodium hydroxide; oxalyl dichloride; ethylmagnesium chloride; sodium hydride; In 1,4-dioxane; ethanol; water;
DOI:10.1021/jm00039a015

Reference yield:

: 59777-95-6
(2RS,4R)-2-(pyridin-3-yl)-4-thiazolidine-carboxylic acid

: 1027527-06-5
(R)-4-[6-Benzyloxy-1-(morpholine-4-carbonyl)-1H-indole-3-carbonyl]-2-pyridin-3-yl-thiazolidine-3-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 80 percent / NaOH / dioxane / 19 h

2: 1.) NaH, 2.) oxalyl chloride / 1.) CH₂Cl₂, until gas evolution ceased, 2.) CH₂Cl₂, RT, 30 min

3: 1.) ethylmagnesium chloride / 1.) benzene, ether, 20 min, 2.) benzene, ether, CH₂Cl₂, RT, 3 h

4: 1.) KOH / 1.) DME, 0 deg C, 10 min, 2.) DME, RT, 30 min

With potassium hydroxide; sodium hydroxide; oxalyl dichloride; ethylmagnesium chloride; sodium hydride; In 1,4-dioxane;
DOI:10.1021/jm00039a015

Reference yield:

: (2RS,4R)-3-tert-butoxycarbonyl-2-(pyridin-3-yl)-4-thiazolidinecarboxylic acid

: 1027527-06-5
(R)-4-[6-Benzyloxy-1-(morpholine-4-carbonyl)-1H-indole-3-carbonyl]-2-pyridin-3-yl-thiazolidine-3-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) NaH, 2.) oxalyl chloride / 1.) CH₂Cl₂, until gas evolution ceased, 2.) CH₂Cl₂, RT, 30 min

2: 1.) ethylmagnesium chloride / 1.) benzene, ether, 20 min, 2.) benzene, ether, CH₂Cl₂, RT, 3 h

3: 1.) KOH / 1.) DME, 0 deg C, 10 min, 2.) DME, RT, 30 min

With potassium hydroxide; oxalyl dichloride; ethylmagnesium chloride; sodium hydride;
DOI:10.1021/jm00039a015