(1S,7bR)-2-Oxo-3-phenylselanyl-1-(trityl-amino)-1,3,4,7b-tetrahydro-2H-2a,6,7,7a-tetraaza-cyclobuta[e]indene-3-carboxylic acid tert-butyl ester

Base Information

Chemical Name:(1S,7bR)-2-Oxo-3-phenylselanyl-1-(trityl-amino)-1,3,4,7b-tetrahydro-2H-2a,6,7,7a-tetraaza-cyclobuta[e]indene-3-carboxylic acid tert-butyl ester
CAS No.:78905-45-0
Molecular Formula:C₃₇H₃₅N₅O₃Se
Molecular Weight:676.677
Hs Code.:

(1S,7bR)-2-Oxo-3-phenylselanyl-1-(trityl-amino)-1,3,4,7b-tetrahydro-2H-2a,6,7,7a-tetraaza-cyclobuta[e]indene-3-carboxylic acid tert-butyl ester

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Chemical Property of (1S,7bR)-2-Oxo-3-phenylselanyl-1-(trityl-amino)-1,3,4,7b-tetrahydro-2H-2a,6,7,7a-tetraaza-cyclobuta[e]indene-3-carboxylic acid tert-butyl ester

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Technology Process of (1S,7bR)-2-Oxo-3-phenylselanyl-1-(trityl-amino)-1,3,4,7b-tetrahydro-2H-2a,6,7,7a-tetraaza-cyclobuta[e]indene-3-carboxylic acid tert-butyl ester

There total 7 articles about (1S,7bR)-2-Oxo-3-phenylselanyl-1-(trityl-amino)-1,3,4,7b-tetrahydro-2H-2a,6,7,7a-tetraaza-cyclobuta[e]indene-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:

: 34837-55-3
Phenylselenyl bromide

: 78905-44-9,78963-74-3
t-butyl (8S,8aR)-4,5,7,8-tetrahydro-7-oxo-8-triphenyllmethylamino-8aH-azeto<1,2-a>-v-triazolo<3,4-c>pyrimidine-5-carboxylate

: 78905-45-0
(1S,7bR)-2-Oxo-3-phenylselanyl-1-(trityl-amino)-1,3,4,7b-tetrahydro-2H-2a,6,7,7a-tetraaza-cyclobuta[e]indene-3-carboxylic acid tert-butyl ester

Guidance literature:: With lithium hexamethyldisilazane; In tetrahydrofuran; hexane; at -76 ℃; for 0.333333h;
DOI:10.1039/P19810002544

Reference yield:

: 5292-43-3
bromoacetic acid tert-butyl ester

: 78905-45-0
(1S,7bR)-2-Oxo-3-phenylselanyl-1-(trityl-amino)-1,3,4,7b-tetrahydro-2H-2a,6,7,7a-tetraaza-cyclobuta[e]indene-3-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 10 g / potassium carbonate / dimethylformamide / 20 h / Ambient temperature

2: chlorine / CCl₄ / 1.5 h / -20 - 0 °C

3: 6.11 g / sodium azide / dimethylformamide / 18 h / Ambient temperature

4: 350 mg / litium hexamethyldisilazane / tetrahydrofuran; hexane / 0.5 h / -76 °C

5: 86 percent / toluene / 8 h / Heating

6: 448 mg / lithium hexamethyldisilazane / tetrahydrofuran; hexane / 0.33 h / -76 °C

With sodium azide; chlorine; potassium carbonate; lithium hexamethyldisilazane; In tetrahydrofuran; tetrachloromethane; hexane; N,N-dimethyl-formamide; toluene;
DOI:10.1039/P19810002544

Reference yield:

: 59461-72-2
(3R,4R)-4-methylthio-3-triphenylmethylaminoazetidin-2-one

: 78905-45-0
(1S,7bR)-2-Oxo-3-phenylselanyl-1-(trityl-amino)-1,3,4,7b-tetrahydro-2H-2a,6,7,7a-tetraaza-cyclobuta[e]indene-3-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 10 g / potassium carbonate / dimethylformamide / 20 h / Ambient temperature

2: chlorine / CCl₄ / 1.5 h / -20 - 0 °C

3: 6.11 g / sodium azide / dimethylformamide / 18 h / Ambient temperature

4: 350 mg / litium hexamethyldisilazane / tetrahydrofuran; hexane / 0.5 h / -76 °C

5: 86 percent / toluene / 8 h / Heating

6: 448 mg / lithium hexamethyldisilazane / tetrahydrofuran; hexane / 0.33 h / -76 °C

With sodium azide; chlorine; potassium carbonate; lithium hexamethyldisilazane; In tetrahydrofuran; tetrachloromethane; hexane; N,N-dimethyl-formamide; toluene;
DOI:10.1039/P19810002544