N,N-dimethyl 2-(p-methoxyphenyl)-3-(trans-2-methoxycarbonylethenyl)-4-trimethylsilyl-1H-pyrrole-1-sulfonamide

Base Information

Chemical Name:N,N-dimethyl 2-(p-methoxyphenyl)-3-(trans-2-methoxycarbonylethenyl)-4-trimethylsilyl-1H-pyrrole-1-sulfonamide
CAS No.:284663-48-5
Molecular Formula:C₂₀H₂₈N₂O₅SSi
Molecular Weight:436.604
Hs Code.:

Synonyms:N,N-dimethyl 2-(p-methoxyphenyl)-3-(trans-2-methoxycarbonylethenyl)-4-trimethylsilyl-1H-pyrrole-1-sulfonamide

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Chemical Property of N,N-dimethyl 2-(p-methoxyphenyl)-3-(trans-2-methoxycarbonylethenyl)-4-trimethylsilyl-1H-pyrrole-1-sulfonamide

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Technology Process of N,N-dimethyl 2-(p-methoxyphenyl)-3-(trans-2-methoxycarbonylethenyl)-4-trimethylsilyl-1H-pyrrole-1-sulfonamide

There total 3 articles about N,N-dimethyl 2-(p-methoxyphenyl)-3-(trans-2-methoxycarbonylethenyl)-4-trimethylsilyl-1H-pyrrole-1-sulfonamide 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%

: 5720-07-0
4-methoxyphenylboronic acid

: 284663-47-4
N,N-dimethyl 2-iodo-3-(trans-2-methoxycarbonylethenyl)-4-trimethylsilyl-1H-pyrrole-1-sulfonamide

: 284663-48-5
N,N-dimethyl 2-(p-methoxyphenyl)-3-(trans-2-methoxycarbonylethenyl)-4-trimethylsilyl-1H-pyrrole-1-sulfonamide

Guidance literature:: With tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium sulfate; In methanol; toluene; at 90 - 100 ℃; for 2h;
DOI:10.1021/jo9915224

Reference yield:

: 284663-67-8
N,N-dimethyl 2,4-bis(trimethylsilyl)-3-bromo-1H-pyrrole-1-sulfonamide

: 284663-48-5
N,N-dimethyl 2-(p-methoxyphenyl)-3-(trans-2-methoxycarbonylethenyl)-4-trimethylsilyl-1H-pyrrole-1-sulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent / Et₃N; PdCl₂(PPh₃)2 / dimethylformamide / 5 h / 110 °C

2: 90 percent / CF₃CO₂Ag; I₂ / tetrahydrofuran / 2 h / -78 °C

3: 100 percent / Pd(PPh₃)4; Na₂SO₄ / methanol; toluene / 2 h / 90 - 100 °C

With bis-triphenylphosphine-palladium(II) chloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; iodine; silver trifluoroacetate; sodium sulfate; triethylamine; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; toluene; 1: Substitution / 2: Iodination / 3: Phenylation;
DOI:10.1021/jo9915224

Reference yield:

: 284663-46-3
N,N-dimethyl 2,4-bis(trimethylsilyl)-3-(trans-2-methoxycarbonylethenyl)-1H-pyrrole-1-sulfonamide

: 284663-48-5
N,N-dimethyl 2-(p-methoxyphenyl)-3-(trans-2-methoxycarbonylethenyl)-4-trimethylsilyl-1H-pyrrole-1-sulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / CF₃CO₂Ag; I₂ / tetrahydrofuran / 2 h / -78 °C

2: 100 percent / Pd(PPh₃)4; Na₂SO₄ / methanol; toluene / 2 h / 90 - 100 °C

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; iodine; silver trifluoroacetate; sodium sulfate; In tetrahydrofuran; methanol; toluene; 1: Iodination / 2: Phenylation;
DOI:10.1021/jo9915224