C₃₅H₄₉N₃O₅

Base Information

Chemical Name:C₃₅H₄₉N₃O₅
CAS No.:956223-85-1
Molecular Formula:C₃₅H₄₉N₃O₅
Molecular Weight:591.791
Hs Code.:

C<sub>35</sub>H<sub>49</sub>N<sub>3</sub>O<sub>5</sub>

Synonyms:

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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 C₃₅H₄₉N₃O₅

Chemical Property:

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Technology Process of C₃₅H₄₉N₃O₅

There total 25 articles about C₃₅H₄₉N₃O₅ 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:

: C₃₆H₅₂O₈S

: 956223-85-1
C₃₅H₄₉N₃O₅

Guidance literature:: With sodium azide; In N,N-dimethyl-formamide; at 90 ℃;
DOI:10.1055/s-2007-985585

Reference yield:

: 869487-89-8
(S)-3-methyl-6-(trimethylsilyl)hex-5-ynal

: 956223-85-1
C₃₅H₄₉N₃O₅

Guidance literature:: Multi-step reaction with 10 steps

1: n-BuLi / -78 °C

2: Dess-Martin periodinane; NaHCO₃ / 0 - 20 °C

3: 96 percent / i-Pr₂NEt; LiCl / acetonitrile / 20 °C

4: 92 percent / AD-mix α; MeSO2NH2; NaHCO3 / 2-methyl-propan-2-ol; H2O / 0 °C

5: 95 percent / PPTS / CH₂Cl₂ / 0 - 20 °C

6: K-selectride / tetrahydrofuran / -78 °C

7: NaHMDS / tetrahydrofuran; dimethylformamide / 0 °C

8: TBAF / tetrahydrofuran / 0 - 20 °C

9: Et₃N / CH₂Cl₂ / 0 °C

10: NaN₃ / dimethylformamide / 90 °C

With AD-mix-α; n-butyllithium; sodium azide; methanesulfonamide; tetrabutyl ammonium fluoride; sodium hexamethyldisilazane; pyridinium p-toluenesulfonate; sodium hydrogencarbonate; potassium tri-sec-butyl-borohydride; Dess-Martin periodane; triethylamine; N-ethyl-N,N-diisopropylamine; lithium chloride; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile; tert-butyl alcohol; 4: Sharpless asymmetric dihydroxylation;
DOI:10.1055/s-2007-985585

Reference yield:

: 956223-72-6
C₃₃H₄₄O₄Si

: 956223-85-1
C₃₅H₄₉N₃O₅

Guidance literature:: Multi-step reaction with 8 steps

1: 96 percent / i-Pr₂NEt; LiCl / acetonitrile / 20 °C

2: 92 percent / AD-mix α; MeSO2NH2; NaHCO3 / 2-methyl-propan-2-ol; H2O / 0 °C

3: 95 percent / PPTS / CH₂Cl₂ / 0 - 20 °C

4: K-selectride / tetrahydrofuran / -78 °C

5: NaHMDS / tetrahydrofuran; dimethylformamide / 0 °C

6: TBAF / tetrahydrofuran / 0 - 20 °C

7: Et₃N / CH₂Cl₂ / 0 °C

8: NaN₃ / dimethylformamide / 90 °C

With AD-mix-α; sodium azide; methanesulfonamide; tetrabutyl ammonium fluoride; sodium hexamethyldisilazane; pyridinium p-toluenesulfonate; sodium hydrogencarbonate; potassium tri-sec-butyl-borohydride; triethylamine; N-ethyl-N,N-diisopropylamine; lithium chloride; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile; tert-butyl alcohol; 2: Sharpless asymmetric dihydroxylation;
DOI:10.1055/s-2007-985585