2-(tert-butoxycarbonylamino-methyl)-8-((E)-styryl)-1H-pyrrolo[2,3-f]isoquinoline-3-carboxylic acid tert-butyl ester

Base Information

Chemical Name:2-(tert-butoxycarbonylamino-methyl)-8-((E)-styryl)-1H-pyrrolo[2,3-f]isoquinoline-3-carboxylic acid tert-butyl ester
CAS No.:1010104-03-6
Molecular Formula:C₃₀H₃₃N₃O₄
Molecular Weight:499.61
Hs Code.:

Synonyms:2-(tert-butoxycarbonylamino-methyl)-8-((E)-styryl)-1H-pyrrolo[2,3-f]isoquinoline-3-carboxylic acid tert-butyl ester

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Chemical Property of 2-(tert-butoxycarbonylamino-methyl)-8-((E)-styryl)-1H-pyrrolo[2,3-f]isoquinoline-3-carboxylic acid tert-butyl ester

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Technology Process of 2-(tert-butoxycarbonylamino-methyl)-8-((E)-styryl)-1H-pyrrolo[2,3-f]isoquinoline-3-carboxylic acid tert-butyl ester

There total 7 articles about 2-(tert-butoxycarbonylamino-methyl)-8-((E)-styryl)-1H-pyrrolo[2,3-f]isoquinoline-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:

: 1010104-02-5
2-(tert-butoxycarbonylamino-methyl)-8-chloro-1H-pyrrolo[2,3-f]isoquinoline-3-carboxylic acid tert-butyl ester

: 6783-05-7
trans-2-phenylvinylboronic acid

: 1010104-03-6
2-(tert-butoxycarbonylamino-methyl)-8-((E)-styryl)-1H-pyrrolo[2,3-f]isoquinoline-3-carboxylic acid tert-butyl ester

Guidance literature:: With potassium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In water; N,N-dimethyl-formamide; at 90 ℃; for 1.5h;

Reference yield:

: 1694-31-1
tert-butyl acetoacetate

: 1010104-03-6
2-(tert-butoxycarbonylamino-methyl)-8-((E)-styryl)-1H-pyrrolo[2,3-f]isoquinoline-3-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: acetic acid / 4 h / 50 °C

2: copper diacetate / palladium diacetate / N,N-dimethyl-formamide / 0.17 h / 60 - 120 °C

3: dmap / diethylene glycol dimethyl ether / 0.67 h / 120 °C

4: N-Bromosuccinimide / dibenzoyl peroxide / tetrachloromethane / 2.5 h / Heating / reflux

5: ammonia / 1,4-dioxane; water / 0.17 h / 100 °C

6: potassium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / water; N,N-dimethyl-formamide / 1.5 h / 90 °C

With N-Bromosuccinimide; ammonia; copper diacetate; potassium carbonate; acetic acid; dmap; palladium diacetate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; dibenzoyl peroxide; In 1,4-dioxane; tetrachloromethane; diethylene glycol dimethyl ether; water; N,N-dimethyl-formamide;

Reference yield:

: 1010103-98-6
(E)-3-(3-chloroisoquinolin-5-ylamino)-but-2-enoic acid tert-butyl ester

: 1010104-03-6
2-(tert-butoxycarbonylamino-methyl)-8-((E)-styryl)-1H-pyrrolo[2,3-f]isoquinoline-3-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: copper diacetate / palladium diacetate / N,N-dimethyl-formamide / 0.17 h / 60 - 120 °C

2: dmap / diethylene glycol dimethyl ether / 0.67 h / 120 °C

3: N-Bromosuccinimide / dibenzoyl peroxide / tetrachloromethane / 2.5 h / Heating / reflux

4: ammonia / 1,4-dioxane; water / 0.17 h / 100 °C

5: potassium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / water; N,N-dimethyl-formamide / 1.5 h / 90 °C

With N-Bromosuccinimide; ammonia; copper diacetate; potassium carbonate; dmap; palladium diacetate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; dibenzoyl peroxide; In 1,4-dioxane; tetrachloromethane; diethylene glycol dimethyl ether; water; N,N-dimethyl-formamide;