tert-butyl 4-(2-benzylthiazol-5-yl)piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-(2-benzylthiazol-5-yl)piperidine-1-carboxylate
CAS No.:301221-60-3
Molecular Formula:C₂₀H₂₆N₂O₂S
Molecular Weight:358.505
Hs Code.:
Mol file:301221-60-3.mol

Synonyms:tert-butyl 4-(2-benzylthiazol-5-yl)piperidine-1-carboxylate

Suppliers and Price of tert-butyl 4-(2-benzylthiazol-5-yl)piperidine-1-carboxylate

Supply Marketing:

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

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Total 1 raw suppliers

Chemical Property of tert-butyl 4-(2-benzylthiazol-5-yl)piperidine-1-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of tert-butyl 4-(2-benzylthiazol-5-yl)piperidine-1-carboxylate

There total 8 articles about tert-butyl 4-(2-benzylthiazol-5-yl)piperidine-1-carboxylate 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:

: 288-47-1
1,3-thiazole

: 301221-60-3
1-t-butyloxycarbonyl-4-(2-benzyl-thiazol-5-yl)piperidine

Guidance literature:

Reference yield:

: 19172-47-5,94367-93-8
Lawessons reagent

: ethyl acetate n-hexane

: 301221-59-0
1-t-butyloxycarbonyl-4-(2-phenylacetamido)acetyl-piperidine

: 301221-60-3
1-t-butyloxycarbonyl-4-(2-benzyl-thiazol-5-yl)piperidine

Guidance literature:: In dichloromethane; ethyl acetate; toluene;

Reference yield:

: 137076-22-3
tert butyl 4-formylpiperidine-1-carboxylate

: 301221-60-3
1-t-butyloxycarbonyl-4-(2-benzyl-thiazol-5-yl)piperidine

Guidance literature:: Multi-step reaction with 5 steps

1: DBU / tetrahydrofuran

2: H₂ / Pd/C / methanol

3: DCC; DMAP / CH₂Cl₂

4: chromic acid / diethyl ether

5: Lawesson's reagent

With Lawessons reagent; dmap; hydrogen; chromic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; dicyclohexyl-carbodiimide; palladium on activated charcoal; In tetrahydrofuran; methanol; diethyl ether; dichloromethane;
DOI:10.1016/j.bmcl.2004.04.078