trans-3-chloro-benzo[b]thiophene-2-carboxylic acid (4'-cyano-4-methoxy-biphenyl-3-ylmethyl)-(4-methylamino-cyclohexyl)-amide hydrochloride

Base Information

Chemical Name:trans-3-chloro-benzo[b]thiophene-2-carboxylic acid (4'-cyano-4-methoxy-biphenyl-3-ylmethyl)-(4-methylamino-cyclohexyl)-amide hydrochloride
CAS No.:945997-16-0
Molecular Formula:C₃₁H₃₀ClN₃O₂S*ClH
Molecular Weight:580.578
Hs Code.:

trans-3-chloro-benzo[b]thiophene-2-carboxylic acid (4'-cyano-4-methoxy-biphenyl-3-ylmethyl)-(4-methylamino-cyclohexyl)-amide hydrochloride

Synonyms:trans-3-chloro-benzo[b]thiophene-2-carboxylic acid (4'-cyano-4-methoxy-biphenyl-3-ylmethyl)-(4-methylamino-cyclohexyl)-amide hydrochloride

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Chemical Property of trans-3-chloro-benzo[b]thiophene-2-carboxylic acid (4'-cyano-4-methoxy-biphenyl-3-ylmethyl)-(4-methylamino-cyclohexyl)-amide hydrochloride

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Technology Process of trans-3-chloro-benzo[b]thiophene-2-carboxylic acid (4'-cyano-4-methoxy-biphenyl-3-ylmethyl)-(4-methylamino-cyclohexyl)-amide hydrochloride

There total 7 articles about trans-3-chloro-benzo[b]thiophene-2-carboxylic acid (4'-cyano-4-methoxy-biphenyl-3-ylmethyl)-(4-methylamino-cyclohexyl)-amide hydrochloride 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: 100.0%

: 945997-14-8
trans-tert-butyl {4-[(3-chloro-benzo[b]thiophene-2-carbonyl)-(4'-cyano-4-methoxy-biphenyl-5-ylmethyl)-amino]-cyclohexyl}-methyl-carbamate

: 945997-16-0
trans-3-chloro-benzo[b]thiophene-2-carboxylic acid (4'-cyano-4-methoxy-biphenyl-3-ylmethyl)-(4-methylamino-cyclohexyl)-amide hydrochloride

Guidance literature:: With hydrogenchloride; ethanol; water; In dichloromethane; at 20 ℃; for 3 - 4h;

Reference yield:

: 15803-59-5,1932261-28-3,38362-02-6
(1r,4r)-N¹-methylcyclohexane-1,4-diamine

: 945997-16-0
trans-3-chloro-benzo[b]thiophene-2-carboxylic acid (4'-cyano-4-methoxy-biphenyl-3-ylmethyl)-(4-methylamino-cyclohexyl)-amide hydrochloride

Guidance literature:: Multi-step reaction with 5 steps

1.1: benzaldehyde / toluene / 6 h / Heating / reflux

1.2: 3.25 h / 20 °C

2.1: acetic acid / tetrahydrofuran; methanol; toluene / 4 h / 20 °C

2.2: 1 h

3.1: caesium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / ethanol; toluene / 0.5 - 1.5 h / 80 - 120 °C / microwave irradiation

4.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 16 h / 0 - 20 °C

5.1: hydrogenchloride; ethanol; water / dichloromethane / 3 - 4 h / 20 °C

With hydrogenchloride; ethanol; water; caesium carbonate; benzaldehyde; acetic acid; N-ethyl-N,N-diisopropylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; methanol; ethanol; dichloromethane; toluene; 3.1: Suzuki Coupling;

Reference yield:

: 566172-79-0
trans-N-methyl-N-tert-butoxycarbonyl-1,4-diaminocyclohexane

: 945997-16-0
trans-3-chloro-benzo[b]thiophene-2-carboxylic acid (4'-cyano-4-methoxy-biphenyl-3-ylmethyl)-(4-methylamino-cyclohexyl)-amide hydrochloride

Guidance literature:: Multi-step reaction with 4 steps

1.1: acetic acid / tetrahydrofuran; methanol; toluene / 4 h / 20 °C

1.2: 1 h

2.1: caesium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / ethanol; toluene / 0.5 - 1.5 h / 80 - 120 °C / microwave irradiation

3.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 16 h / 0 - 20 °C

4.1: hydrogenchloride; ethanol; water / dichloromethane / 3 - 4 h / 20 °C

With hydrogenchloride; ethanol; water; caesium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; methanol; ethanol; dichloromethane; toluene; 2.1: Suzuki Coupling;