(2-tert-butoxycarbonylamino-4-tert-butyl-5-mercapto-phenyl)-carbamic acid tert-butyl ester

Base Information

Chemical Name:(2-tert-butoxycarbonylamino-4-tert-butyl-5-mercapto-phenyl)-carbamic acid tert-butyl ester
CAS No.:261712-35-0
Molecular Formula:C₂₀H₃₂N₂O₄S
Molecular Weight:396.551
Hs Code.:

Synonyms:(2-tert-butoxycarbonylamino-4-tert-butyl-5-mercapto-phenyl)-carbamic acid tert-butyl ester

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Chemical Property of (2-tert-butoxycarbonylamino-4-tert-butyl-5-mercapto-phenyl)-carbamic acid tert-butyl ester

Chemical Property:

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Technology Process of (2-tert-butoxycarbonylamino-4-tert-butyl-5-mercapto-phenyl)-carbamic acid tert-butyl ester

There total 8 articles about (2-tert-butoxycarbonylamino-4-tert-butyl-5-mercapto-phenyl)-carbamic 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:

: sodium hydrogensulfide

: 261712-13-4
(2-tert-butoxycarbonylamino-4-tert-butyl-5-thiocyanato-phenyl)-carbamic acid tert-butyl ester

: 261712-35-0
(2-tert-butoxycarbonylamino-4-tert-butyl-5-mercapto-phenyl)-carbamic acid tert-butyl ester

Guidance literature:: With sodium borohydrid; acetic acid; In methanol; water;

Reference yield:

: 261712-13-4
(2-tert-butoxycarbonylamino-4-tert-butyl-5-thiocyanato-phenyl)-carbamic acid tert-butyl ester

: 261712-35-0
(2-tert-butoxycarbonylamino-4-tert-butyl-5-mercapto-phenyl)-carbamic acid tert-butyl ester

Guidance literature:: With sodium tetrahydroborate; sodium hydrogensulfide; In methanol; at 20 ℃; for 16h;
DOI:10.1021/ol0056170

Reference yield:

: 5369-19-7
3-tert-butylaniline

: 261712-35-0
(2-tert-butoxycarbonylamino-4-tert-butyl-5-mercapto-phenyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: KNO₃ / 0 - 20 °C

2: aq. K₂CO₃ / methanol / 16 h / 20 °C

3: 90 percent / NaBr; Br₂ / 0 - 20 °C

4: 95 percent / H₂ / Raney nickel / tetrahydrofuran / 16 h / 2585.81 Torr

5: 98 percent / ethyl acetate; hexane / 16 h / Heating

6: aq. NaSH; NaBH₄ / methanol / 16 h / 20 °C

With sodium tetrahydroborate; sodium hydrogensulfide; hydrogen; bromine; potassium carbonate; potassium nitrate; sodium bromide; nickel; In tetrahydrofuran; methanol; hexane; ethyl acetate; 1: Nitration / 2: Hydrolysis / 3: thiocyanation / 4: Reduction / 5: Acylation / 6: Reduction;
DOI:10.1021/ol0056170