C₅₈H₇₈N₁₂O₁₃S₃

Base Information

Chemical Name:C₅₈H₇₈N₁₂O₁₃S₃
CAS No.:1453168-14-3
Molecular Formula:C₅₈H₇₈N₁₂O₁₃S₃
Molecular Weight:1247.53
Hs Code.:

C<sub>58</sub>H<sub>78</sub>N<sub>12</sub>O<sub>13</sub>S<sub>3</sub>

Synonyms:C₅₈H₇₈N₁₂O₁₃S₃

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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 C₅₈H₇₈N₁₂O₁₃S₃

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Technology Process of C₅₈H₇₈N₁₂O₁₃S₃

There total 9 articles about C₅₈H₇₈N₁₂O₁₃S₃ 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: 39.0%

: 1453168-13-2
C₃₇H₄₃N₉O₆S₂

: 365441-71-0
4,7,10,13-tetraoxa-16-azaheneicosanoic acid 21-[(3aS,4S,6aR)-hexahydro-2-oxo-1H-thieno[3,4-d]imidazol-4-yl]-17-oxo-2,5-dioxo-1-pyrrolidinyl ester

: 1453168-14-3
C₅₈H₇₈N₁₂O₁₃S₃

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; for 2h; Inert atmosphere;
DOI:10.1021/ol401749p

Reference yield:

: 96929-06-5
ethyl 2-<(S)-1-(N-t-butoxycarbonyl)aminoethyl>thiazole-4-carboxylate

: 1453168-14-3
C₅₈H₇₈N₁₂O₁₃S₃

Guidance literature:: Multi-step reaction with 9 steps

1: trifluoroacetic acid; methoxybenzene / dichloromethane

2: N-ethyl-N,N-diisopropylamine; HATU; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholin-4-ium / dichloromethane / 1 h / 20 °C / Inert atmosphere

3: trifluoroacetic acid; methoxybenzene / dichloromethane

4: N-ethyl-N,N-diisopropylamine; HATU; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholin-4-ium; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide / dichloromethane / 1 h / 20 °C / Inert atmosphere

5: lithium hydroxide; dihydrogen peroxide / ethanol

6: trifluoroacetic acid; methoxybenzene / dichloromethane

7: N-ethyl-N,N-diisopropylamine; HATU; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholin-4-ium; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide / dichloromethane / 1 h / 20 °C / Inert atmosphere

8: hydrogen bromide; acetic acid / 1 h

9: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / Inert atmosphere

With hydrogen bromide; dihydrogen peroxide; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholin-4-ium; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; acetic acid; methoxybenzene; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; N-ethyl-N,N-diisopropylamine; HATU; trifluoroacetic acid; lithium hydroxide; In ethanol; dichloromethane;
DOI:10.1021/ol401749p

Reference yield:

: 1453168-06-3
C₅₂H₆₃N₉O₁₁S₂

: 1453168-14-3
C₅₈H₇₈N₁₂O₁₃S₃

Guidance literature:: Multi-step reaction with 5 steps

1: lithium hydroxide; dihydrogen peroxide / ethanol

2: trifluoroacetic acid; methoxybenzene / dichloromethane

3: N-ethyl-N,N-diisopropylamine; HATU; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholin-4-ium; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide / dichloromethane / 1 h / 20 °C / Inert atmosphere

4: hydrogen bromide; acetic acid / 1 h

5: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / Inert atmosphere

With hydrogen bromide; dihydrogen peroxide; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholin-4-ium; acetic acid; methoxybenzene; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; N-ethyl-N,N-diisopropylamine; HATU; trifluoroacetic acid; lithium hydroxide; In ethanol; dichloromethane;
DOI:10.1021/ol401749p