methanesulfonic acid 2-{4-benzylamino-2-[(5,6,7-trimethoxy-1H-indole-2-carbonyl)-amino]-naphthalen-1-yl}-ethyl ester

Base Information

Chemical Name:methanesulfonic acid 2-{4-benzylamino-2-[(5,6,7-trimethoxy-1H-indole-2-carbonyl)-amino]-naphthalen-1-yl}-ethyl ester
CAS No.:855299-70-6
Molecular Formula:C₃₂H₃₃N₃O₇S
Molecular Weight:603.696
Hs Code.:

methanesulfonic acid 2-{4-benzylamino-2-[(5,6,7-trimethoxy-1<i>H</i>-indole-2-carbonyl)-amino]-naphthalen-1-yl}-ethyl ester

Synonyms:methanesulfonic acid 2-{4-benzylamino-2-[(5,6,7-trimethoxy-1H-indole-2-carbonyl)-amino]-naphthalen-1-yl}-ethyl ester

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Chemical Property of methanesulfonic acid 2-{4-benzylamino-2-[(5,6,7-trimethoxy-1H-indole-2-carbonyl)-amino]-naphthalen-1-yl}-ethyl ester

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Technology Process of methanesulfonic acid 2-{4-benzylamino-2-[(5,6,7-trimethoxy-1H-indole-2-carbonyl)-amino]-naphthalen-1-yl}-ethyl ester

There total 7 articles about methanesulfonic acid 2-{4-benzylamino-2-[(5,6,7-trimethoxy-1H-indole-2-carbonyl)-amino]-naphthalen-1-yl}-ethyl ester 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:

: 855299-62-6
2-[4-(N-benzylamino)-2-nitronaphthalen-1-yl]ethanol

: 855299-70-6
methanesulfonic acid 2-{4-benzylamino-2-[(5,6,7-trimethoxy-1H-indole-2-carbonyl)-amino]-naphthalen-1-yl}-ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 55 percent / pyridine / 20 °C

2: H₂ / PtO₂ / tetrahydrofuran / 2 h / 20 °C / 2844.31 Torr

3: 1.1 g / PyBOP; iPr₂NEt / CH₂Cl₂ / 48 h / 20 °C

4: K₂CO₃ / methanol; tetrahydrofuran / 20 °C

5: 700 mg / Et₃N / CH₂Cl₂ / 1 h / cooling

With pyridine; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; hydrogen; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; platinum(IV) oxide; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/jm050179u

Reference yield:

: 855299-61-5
[4-(N-benzylamino)-2-nitronaphthalen-1-yl]acetic acid

: 855299-70-6
methanesulfonic acid 2-{4-benzylamino-2-[(5,6,7-trimethoxy-1H-indole-2-carbonyl)-amino]-naphthalen-1-yl}-ethyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 55 percent / BH₃ / tetrahydrofuran

2: 55 percent / pyridine / 20 °C

3: H₂ / PtO₂ / tetrahydrofuran / 2 h / 20 °C / 2844.31 Torr

4: 1.1 g / PyBOP; iPr₂NEt / CH₂Cl₂ / 48 h / 20 °C

5: K₂CO₃ / methanol; tetrahydrofuran / 20 °C

6: 700 mg / Et₃N / CH₂Cl₂ / 1 h / cooling

With pyridine; borane; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; hydrogen; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; platinum(IV) oxide; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/jm050179u

Reference yield:

: ethyl [4-(N-benzylamino)-2-nitronaphthalen-1-yl]acetate

: 855299-70-6
methanesulfonic acid 2-{4-benzylamino-2-[(5,6,7-trimethoxy-1H-indole-2-carbonyl)-amino]-naphthalen-1-yl}-ethyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 89 percent / aq. NaOH / ethanol / 2 h / Heating

2: 55 percent / BH₃ / tetrahydrofuran

3: 55 percent / pyridine / 20 °C

4: H₂ / PtO₂ / tetrahydrofuran / 2 h / 20 °C / 2844.31 Torr

5: 1.1 g / PyBOP; iPr₂NEt / CH₂Cl₂ / 48 h / 20 °C

6: K₂CO₃ / methanol; tetrahydrofuran / 20 °C

7: 700 mg / Et₃N / CH₂Cl₂ / 1 h / cooling

With pyridine; sodium hydroxide; borane; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; hydrogen; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; platinum(IV) oxide; In tetrahydrofuran; methanol; ethanol; dichloromethane;
DOI:10.1021/jm050179u