{1-[(benzhydryl-sulfamoyl)-methyl]-2-methyl-propyl}-carbamic acid tert-butyl ester

Base Information

Chemical Name:{1-[(benzhydryl-sulfamoyl)-methyl]-2-methyl-propyl}-carbamic acid tert-butyl ester
CAS No.:503625-36-3
Molecular Formula:C₂₃H₃₂N₂O₄S
Molecular Weight:432.584
Hs Code.:

{1-[(benzhydryl-sulfamoyl)-methyl]-2-methyl-propyl}-carbamic acid <i>tert</i>-butyl ester

Synonyms:{1-[(benzhydryl-sulfamoyl)-methyl]-2-methyl-propyl}-carbamic acid tert-butyl ester

Suppliers and Price of {1-[(benzhydryl-sulfamoyl)-methyl]-2-methyl-propyl}-carbamic acid tert-butyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemicals and raw materials
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Total 1 raw suppliers

Chemical Property of {1-[(benzhydryl-sulfamoyl)-methyl]-2-methyl-propyl}-carbamic acid tert-butyl ester

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

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Hazard Codes:

MSDS Files:

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Technology Process of {1-[(benzhydryl-sulfamoyl)-methyl]-2-methyl-propyl}-carbamic acid tert-butyl ester

There total 1 articles about {1-[(benzhydryl-sulfamoyl)-methyl]-2-methyl-propyl}-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:

: 91-00-9
Benzhydrylamine

: 212204-34-7
(1S-chlorosulfonylmethyl-2-methylpropyl)carbamic acid, tert-butyl ester

: 503625-36-3
{1-[(benzhydryl-sulfamoyl)-methyl]-2-methyl-propyl}-carbamic acid tert-butyl ester

Guidance literature:: With 1-methoxy-2-methyl-1-trimethylsiloxy-1-propene; polystyrene-bound 4-(N-benzyl-N-methylamino)pyridine; In dichloromethane; at 20 ℃; for 3h;
DOI:10.1002/(SICI)1521-3773(20000303)39:5<916::AID-ANIE916>3.0.CO;2-M

Reference yield:

: 503625-36-3
{1-[(benzhydryl-sulfamoyl)-methyl]-2-methyl-propyl}-carbamic acid tert-butyl ester

: (S)-2-{[1-(2-Hydroxy-phenyl)-meth-(E)-ylidene]-amino}-3-methyl-butane-1-sulfonic acid benzhydryl-amide

Guidance literature:: Multi-step reaction with 2 steps

1: CH₂Cl₂ / 0.5 h / 20 °C

2: polymer-bound dimethylaminopyridine / methanol / 24 h / 20 °C

With polymer-bound dimethylaminopyridine; In methanol; dichloromethane;
DOI:10.1002/1521-3765(20010618)7:12<2628::AID-CHEM26280>3.0.CO;2-7

Reference yield:

: 503625-36-3
{1-[(benzhydryl-sulfamoyl)-methyl]-2-methyl-propyl}-carbamic acid tert-butyl ester

: (S)-2-{[1-(3,5-Dichloro-2-hydroxy-phenyl)-meth-(E)-ylidene]-amino}-3-methyl-butane-1-sulfonic acid benzhydryl-amide

Guidance literature:: Multi-step reaction with 2 steps

1: CH₂Cl₂ / 0.5 h / 20 °C

2: polymer-bound dimethylaminopyridine / methanol / 24 h / 20 °C

With polymer-bound dimethylaminopyridine; In methanol; dichloromethane;
DOI:10.1002/1521-3765(20010618)7:12<2628::AID-CHEM26280>3.0.CO;2-7