C₄₁H₄₉FN₄O₇S

Base Information

Chemical Name:C₄₁H₄₉FN₄O₇S
CAS No.:1311410-69-1
Molecular Formula:C₄₁H₄₉FN₄O₇S
Molecular Weight:760.927
Hs Code.:

C<sub>41</sub>H<sub>49</sub>FN<sub>4</sub>O<sub>7</sub>S

Synonyms:C₄₁H₄₉FN₄O₇S

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Chemical Property of C₄₁H₄₉FN₄O₇S

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Technology Process of C₄₁H₄₉FN₄O₇S

There total 17 articles about C₄₁H₄₉FN₄O₇S 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: 79.0%

: 1311412-03-9
C₃₃H₃₆FN₃O₄S

: 162537-11-3
(S)-2-(methoxycarbonylamino)-3,3-dimethylbutanoic acid

: 1311410-69-1
C₄₁H₄₉FN₄O₇S

Guidance literature:: With triethylamine; HATU; In N,N-dimethyl-formamide; at 20 ℃; for 1h;

Reference yield:

: C₂₁H₂₅N₂O₅^(1-)*Li⁽¹⁺⁾

: 1311410-69-1
C₄₁H₄₉FN₄O₇S

Guidance literature:: Multi-step reaction with 6 steps

1.1: lithium diisopropyl amide / tetrahydrofuran / 2 h / -65 - -60 °C / Inert atmosphere

1.2: 3.25 h / -10 - -5 °C / Inert atmosphere

2.1: bis(norbornadiene)rhodium(l)tetrafluoroborate; (S_P,S′_P)-1,1′-bis[bis(4-methoxy-3,5-dimethylphenyl)phosphino]-2,2′-bis[(R)-α-(dimethylamino)benzyl]ferrocene; hydrogen / isopropyl alcohol / 45 °C / 22502.3 Torr / Inert atmosphere

3.1: potassium hydroxide / tert-Amyl alcohol

4.1: zinc(II) chloride; N,N,N,N,-tetramethylethylenediamine / tetrahydrofuran / 0.5 h / -70 - -60 °C / Inert atmosphere

4.2: 12 h / -70 - -3 °C / Inert atmosphere

5.1: hydrogenchloride / water; Isopropyl acetate / 10.5 h / 5 - 55 °C

6.1: HATU; triethylamine / N,N-dimethyl-formamide / 0.5 h / 25 - 30 °C

With hydrogenchloride; bis(norbornadiene)rhodium(l)tetrafluoroborate; (S_P,S′_P)-1,1′-bis[bis(4-methoxy-3,5-dimethylphenyl)phosphino]-2,2′-bis[(R)-α-(dimethylamino)benzyl]ferrocene; N,N,N,N,-tetramethylethylenediamine; hydrogen; triethylamine; HATU; potassium hydroxide; zinc(II) chloride; lithium diisopropyl amide; In tetrahydrofuran; tert-Amyl alcohol; Isopropyl acetate; water; N,N-dimethyl-formamide; isopropyl alcohol;
DOI:10.1002/adsc.201300074

Reference yield:

: C₂₁H₂₅ClN₂O₄

: 1311410-69-1
C₄₁H₄₉FN₄O₇S

Guidance literature:: Multi-step reaction with 5 steps

1.1: NADH; ketoreductase CDX-022 mutant / tetrahydrofuran; isopropyl alcohol; aq. phosphate buffer / 25 °C / pH 7 / Inert atmosphere; Enzymatic reaction

2.1: potassium hydroxide / tert-Amyl alcohol

3.1: zinc(II) chloride; N,N,N,N,-tetramethylethylenediamine / tetrahydrofuran / 0.5 h / -70 - -60 °C / Inert atmosphere

3.2: 12 h / -70 - -3 °C / Inert atmosphere

4.1: hydrogenchloride / water; Isopropyl acetate / 10.5 h / 5 - 55 °C

5.1: HATU; triethylamine / N,N-dimethyl-formamide / 0.5 h / 25 - 30 °C

With hydrogenchloride; N,N,N,N,-tetramethylethylenediamine; ketoreductase CDX-022 mutant; triethylamine; HATU; NADH; potassium hydroxide; zinc(II) chloride; In tetrahydrofuran; tert-Amyl alcohol; aq. phosphate buffer; Isopropyl acetate; water; N,N-dimethyl-formamide; isopropyl alcohol;
DOI:10.1002/adsc.201300074