2-{N-t-butoxycarbonylamino}-N-{2-[U-13C]phenyl-1-phenylprop-2-yl}acetamide

Base Information

Chemical Name:2-{N-t-butoxycarbonylamino}-N-{2-[U-13C]phenyl-1-phenylprop-2-yl}acetamide
CAS No.:286957-70-8
Molecular Formula:C₂₂H₂₈N₂O₃
Molecular Weight:374.41
Hs Code.:

Synonyms:2-{N-t-butoxycarbonylamino}-N-{2-[U-13C]phenyl-1-phenylprop-2-yl}acetamide

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Chemical Property of 2-{N-t-butoxycarbonylamino}-N-{2-[U-13C]phenyl-1-phenylprop-2-yl}acetamide

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Technology Process of 2-{N-t-butoxycarbonylamino}-N-{2-[U-13C]phenyl-1-phenylprop-2-yl}acetamide

There total 6 articles about 2-{N-t-butoxycarbonylamino}-N-{2-[U-13C]phenyl-1-phenylprop-2-yl}acetamide 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: 86.0%

: 161203-15-2
N-Boc-glycine-pivalic acid mixed anhydride

: 286957-67-3
2-[U-13C]phenyl-1-phenylprop-2-ylamine

: 286957-70-8
2-{N-t-butoxycarbonylamino}-N-{2-[U-13C]phenyl-1-phenylprop-2-yl}acetamide

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃;
DOI:10.1002/(SICI)1099-1344(200005)43:6<533::AID-JLCR338>3.0.CO;2-K

Reference yield:

: 4530-20-5
BOC-glycine

: 286957-70-8
2-{N-t-butoxycarbonylamino}-N-{2-[U-13C]phenyl-1-phenylprop-2-yl}acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / CH₂Cl₂ / 2.5 h / 0 °C

2: 86 percent / triethylamine / CH₂Cl₂ / 0 - 20 °C

With triethylamine; In dichloromethane; 1: Acylation / 2: Acylation;
DOI:10.1002/(SICI)1099-1344(200005)43:6<533::AID-JLCR338>3.0.CO;2-K

Reference yield:

: 1589-82-8
phenylmagnesium bromide

: 286957-70-8
2-{N-t-butoxycarbonylamino}-N-{2-[U-13C]phenyl-1-phenylprop-2-yl}acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: 6.14 g / tetrahydrofuran

2: 42 percent / AcOH; H₂SO₄ / 3.5 h / 16 - 22 °C

3: 2.5 g / conc. HCl / H₂O / 1.75 h / Heating

4: 86 percent / triethylamine / CH₂Cl₂ / 0 - 20 °C

With hydrogenchloride; sulfuric acid; acetic acid; triethylamine; In tetrahydrofuran; dichloromethane; water; 1: Grignard reaction / 2: Substitution / 3: Hydrolysis / 4: Acylation;
DOI:10.1002/(SICI)1099-1344(200005)43:6<533::AID-JLCR338>3.0.CO;2-K