Piv-Proψα(O^βBzl)>Gly-NHiPr

Base Information

Chemical Name:Piv-Proψα(O^βBzl)>Gly-NHiPr
CAS No.:151965-00-3
Molecular Formula:C₂₂H₃₃N₃O₄
Molecular Weight:403.522
Hs Code.:

Piv-Proψ<CO-N<sup>α</sup>(O<sup>β</sup>Bzl)>Gly-NHiPr

Synonyms:Piv-Proψα(O^βBzl)>Gly-NHiPr

Suppliers and Price of Piv-Proψα(O^βBzl)>Gly-NHiPr

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

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Chemical Property of Piv-Proψα(O^βBzl)>Gly-NHiPr

Chemical Property:

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Technology Process of Piv-Proψα(O^βBzl)>Gly-NHiPr

There total 3 articles about Piv-Proψα(O^βBzl)>Gly-NHiPr 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:

: 75726-96-4
2-bromo-N-isopropylacetamide

: 151965-00-3
Piv-Proψα(O^βBzl)>Gly-NHiPr

Guidance literature:: Multi-step reaction with 2 steps

1: HCl, NMM / dimethylformamide / 25 °C

2: DCCI, DMAP / tetrahydrofuran / 0 °C

With 4-methyl-morpholine; hydrogenchloride; dmap; dicyclohexyl-carbodiimide; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/ja00073a002

Reference yield:

: 32909-49-2
N-pivaloyl-L-proline

: 151965-03-6
2-Benzyloxyamino-N-isopropyl-acetamide

: 151965-00-3
Piv-Proψα(O^βBzl)>Gly-NHiPr

Guidance literature:: With dmap; dicyclohexyl-carbodiimide; In tetrahydrofuran; at 0 ℃;
DOI:10.1021/ja00073a002

Reference yield:

: 622-33-3
N-benzyloxyamine

: 151965-00-3
Piv-Proψα(O^βBzl)>Gly-NHiPr

Guidance literature:: Multi-step reaction with 2 steps

1: HCl, NMM / dimethylformamide / 25 °C

2: DCCI, DMAP / tetrahydrofuran / 0 °C

With 4-methyl-morpholine; hydrogenchloride; dmap; dicyclohexyl-carbodiimide; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/ja00073a002