C₂₄H₃₀ClN₃O₄

Base Information

Chemical Name:C₂₄H₃₀ClN₃O₄
CAS No.:935764-66-2
Molecular Formula:C₂₄H₃₀ClN₃O₄
Molecular Weight:459.973
Hs Code.:

C<sub>24</sub>H<sub>30</sub>ClN<sub>3</sub>O<sub>4</sub>

Synonyms:

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Chemical Property of C₂₄H₃₀ClN₃O₄

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Technology Process of C₂₄H₃₀ClN₃O₄

There total 7 articles about C₂₄H₃₀ClN₃O₄ 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:

: 109-01-3
1-methyl-piperazine

: C₂₅H₂₃ClN₂O₇

: 935764-66-2
C₂₄H₃₀ClN₃O₄

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide;

Reference yield:

: 139975-98-7
tert-butyl-(4-hydroxynaphthalen-2-yl)carbamate

: 935764-66-2
C₂₄H₃₀ClN₃O₄

Guidance literature:: Multi-step reaction with 7 steps

1: N-ethyl-N,N-diisopropylamine / dichloromethane

2: N-iodo-succinimide; toluene-4-sulfonic acid / tetrahydrofuran; methanol

3: sodium hydride; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide; mineral oil

4: tri-n-butyl-tin hydride; 2,2'-azobis(isobutyronitrile) / toluene / 80 °C

5: hydrogenchloride / tetrahydrofuran; water; isopropyl alcohol

6: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 0 °C

7: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide

With hydrogenchloride; N-iodo-succinimide; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; tetra-(n-butyl)ammonium iodide; sodium hydride; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; isopropyl alcohol; toluene; mineral oil;

Reference yield:

: 198708-95-1
N-(tert-Butyloxycarbonyl)-4-(methoxymethoxy)-2-naphthylamine

: 935764-66-2
C₂₄H₃₀ClN₃O₄

Guidance literature:: Multi-step reaction with 6 steps

1: N-iodo-succinimide; toluene-4-sulfonic acid / tetrahydrofuran; methanol

2: sodium hydride; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide; mineral oil

3: tri-n-butyl-tin hydride; 2,2'-azobis(isobutyronitrile) / toluene / 80 °C

4: hydrogenchloride / tetrahydrofuran; water; isopropyl alcohol

5: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 0 °C

6: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide

With hydrogenchloride; N-iodo-succinimide; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; tetra-(n-butyl)ammonium iodide; sodium hydride; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide; isopropyl alcohol; toluene; mineral oil;