(+/-)-4-[(3,3-dimethyl-cyclobutyl)-(3-methyl-quinolin-2-ylamino)-methyl]-benzoic acid

Base Information

Chemical Name:(+/-)-4-[(3,3-dimethyl-cyclobutyl)-(3-methyl-quinolin-2-ylamino)-methyl]-benzoic acid
CAS No.:1421348-75-5
Molecular Formula:C₂₄H₂₆N₂O₂
Molecular Weight:374.483
Hs Code.:

Synonyms:(+/-)-4-[(3,3-dimethyl-cyclobutyl)-(3-methyl-quinolin-2-ylamino)-methyl]-benzoic acid

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Chemical Property of (+/-)-4-[(3,3-dimethyl-cyclobutyl)-(3-methyl-quinolin-2-ylamino)-methyl]-benzoic acid

Chemical Property:

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Technology Process of (+/-)-4-[(3,3-dimethyl-cyclobutyl)-(3-methyl-quinolin-2-ylamino)-methyl]-benzoic acid

There total 7 articles about (+/-)-4-[(3,3-dimethyl-cyclobutyl)-(3-methyl-quinolin-2-ylamino)-methyl]-benzoic acid 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:

: 1421348-74-4
(+/-)-4-[(3,3-dimethyl-cyclobutyl)-(3-methyl-quinolin-2-ylamino)-methyl]-benzoic acid ethyl ester

: 1421348-75-5
(+/-)-4-[(3,3-dimethyl-cyclobutyl)-(3-methyl-quinolin-2-ylamino)-methyl]-benzoic acid

Guidance literature:: With sodium hydroxide; In tetrahydrofuran; methanol; at 50 ℃; for 4h;

Reference yield:

: 612-58-8
3-methylquinoline

: 1421348-75-5
(+/-)-4-[(3,3-dimethyl-cyclobutyl)-(3-methyl-quinolin-2-ylamino)-methyl]-benzoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: dihydrogen peroxide; acetic acid / water / 16 h / 80 °C

2: bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / dichloromethane / 28 h / 20 °C

3: sodium hydroxide / tetrahydrofuran; methanol / 4 h / 50 °C

With dihydrogen peroxide; acetic acid; N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; sodium hydroxide; In tetrahydrofuran; methanol; dichloromethane; water;

Reference yield:

: 34970-18-8
3,3-dimethylcyclobutanecarboxylic acid

: 1421348-75-5
(+/-)-4-[(3,3-dimethyl-cyclobutyl)-(3-methyl-quinolin-2-ylamino)-methyl]-benzoic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: oxalyl dichloride / dichloromethane / 4 h / 20 °C

2.1: TurboGrignard / tetrahydrofuran / 2.25 h / -30 °C

2.2: 0.42 h / -30 - -20 °C

2.3: 4.08 h / -40 - 0 °C

3.1: sodium cyanoborohydride; ammonium acetate / methanol / 17 h / 60 °C

4.1: bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / dichloromethane / 28 h / 20 °C

5.1: sodium hydroxide / tetrahydrofuran; methanol / 4 h / 50 °C

With TurboGrignard; oxalyl dichloride; ammonium acetate; sodium cyanoborohydride; N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; sodium hydroxide; In tetrahydrofuran; methanol; dichloromethane;