2-tert-butoxycarbonylamino-5-[2-nitro-4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-pentanoic acid

Base Information

Chemical Name:2-tert-butoxycarbonylamino-5-[2-nitro-4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-pentanoic acid
CAS No.:338735-85-6
Molecular Formula:C₁₈H₂₁F₃N₄O₆
Molecular Weight:446.383
Hs Code.:

2-<i>tert</i>-butoxycarbonylamino-5-[2-nitro-4-(3-trifluoromethyl-3<i>H</i>-diazirin-3-yl)-phenyl]-pentanoic acid

Synonyms:2-tert-butoxycarbonylamino-5-[2-nitro-4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-pentanoic acid

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Chemical Property of 2-tert-butoxycarbonylamino-5-[2-nitro-4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-pentanoic acid

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Technology Process of 2-tert-butoxycarbonylamino-5-[2-nitro-4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-pentanoic acid

There total 5 articles about 2-tert-butoxycarbonylamino-5-[2-nitro-4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-pentanoic acid 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: 97.0%

: 24424-99-5
di-tert-butyl dicarbonate

: 338735-78-7
L-2-amino-5-[4-(1-azi-2,2,2-trifluoroethyl)-2-nitrophenyl]pentanoic acid

: 338735-85-6
2-tert-butoxycarbonylamino-5-[2-nitro-4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-pentanoic acid

Guidance literature:: With triethylamine; In 1,4-dioxane; water; at 20 ℃; for 12h;
DOI:10.3987/com-00-s(i)90

Reference yield:

: 271252-22-3
3-(azi-2,2,2-trifluoroethyl)-6-(3-bromopropyl)-1-nitrobenzene

: 338735-85-6
2-tert-butoxycarbonylamino-5-[2-nitro-4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-pentanoic acid

Guidance literature:: Multi-step reaction with 5 steps

1: 53 percent / NaH / dimethylformamide / 24 h / 20 °C

2: 100 percent / aq. NaOH / ethanol; H₂O / 20 °C

3: dioxane / 1 h / 80 °C

4: 29 percent / aq. NaOH; CoCl₂; Aspergillus genus enzyme / aq. phosphate buffer / 48 h / 35 - 38 °C / pH 6.7

5: 97 percent / Et₃N / dioxane; H₂O / 12 h / 20 °C

With sodium hydroxide; Aspergillus genus enzyme; sodium hydride; triethylamine; In 1,4-dioxane; phosphate buffer; ethanol; water; N,N-dimethyl-formamide;
DOI:10.3987/com-00-s(i)90

Reference yield:

: 338735-77-6
DL-2-acetamido-5-[4-(1-azi-2,2,2-trifluoroethyl)-2-nitrophenyl]pentanoic acid

: 338735-85-6
2-tert-butoxycarbonylamino-5-[2-nitro-4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-pentanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 29 percent / aq. NaOH; CoCl₂; Aspergillus genus enzyme / aq. phosphate buffer / 48 h / 35 - 38 °C / pH 6.7

2: 97 percent / Et₃N / dioxane; H₂O / 12 h / 20 °C

With sodium hydroxide; Aspergillus genus enzyme; triethylamine; In 1,4-dioxane; phosphate buffer; water;
DOI:10.3987/com-00-s(i)90