3-chloro-1-{4-[({1-[(3-methoxy-isoxazole-5-carbonyl)-amino]-cyclopropane-carbonyl}-amino)-methyl]-phenyl}-1H-indole-2-carboxylic acid

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Chemical Name:3-chloro-1-{4-[({1-[(3-methoxy-isoxazole-5-carbonyl)-amino]-cyclopropane-carbonyl}-amino)-methyl]-phenyl}-1H-indole-2-carboxylic acid
CAS No.:1374454-06-4
Molecular Formula:C₂₅H₂₁ClN₄O₆
Molecular Weight:508.918
Hs Code.:

Synonyms:3-chloro-1-{4-[({1-[(3-methoxy-isoxazole-5-carbonyl)-amino]-cyclopropane-carbonyl}-amino)-methyl]-phenyl}-1H-indole-2-carboxylic acid

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Chemical Property of 3-chloro-1-{4-[({1-[(3-methoxy-isoxazole-5-carbonyl)-amino]-cyclopropane-carbonyl}-amino)-methyl]-phenyl}-1H-indole-2-carboxylic acid

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Technology Process of 3-chloro-1-{4-[({1-[(3-methoxy-isoxazole-5-carbonyl)-amino]-cyclopropane-carbonyl}-amino)-methyl]-phenyl}-1H-indole-2-carboxylic acid

There total 7 articles about 3-chloro-1-{4-[({1-[(3-methoxy-isoxazole-5-carbonyl)-amino]-cyclopropane-carbonyl}-amino)-methyl]-phenyl}-1H-indole-2-carboxylic 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: 74.0%

: 1374454-01-9
3-chloro-1-{4-[({1-[(3-methoxy-isoxazole-5-carbonyl)-amino]-cyclopropane-carbonyl}-amino)-methyl]-phenyl}-1H-indole-2-carboxylic acid ethyl ester

: 1374454-06-4
3-chloro-1-{4-[({1-[(3-methoxy-isoxazole-5-carbonyl)-amino]-cyclopropane-carbonyl}-amino)-methyl]-phenyl}-1H-indole-2-carboxylic acid

Guidance literature:: 3-chloro-1-{4-[({1-[(3-methoxy-isoxazole-5-carbonyl)-amino]-cyclopropane-carbonyl}-amino)-methyl]-phenyl}-1H-indole-2-carboxylic acid ethyl ester; With lithium hydroxide monohydrate; water; In tetrahydrofuran; methanol; at 20 ℃;

With hydrogenchloride; In tetrahydrofuran; methanol; water; pH=5;

Reference yield:

: 38343-91-8
3-chloro-1H-indole-2-carboxylic acid ethyl ester

: 1374454-06-4
3-chloro-1-{4-[({1-[(3-methoxy-isoxazole-5-carbonyl)-amino]-cyclopropane-carbonyl}-amino)-methyl]-phenyl}-1H-indole-2-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: N-ethyl-N,N-diisopropylamine / copper diacetate / N,N-dimethyl-formamide / 30 h / 20 °C / Molecular sieve

2.1: hydroxylamine hydrochloride; triethylamine / ethanol / 1 h / 20 °C

3.1: hydrogenchloride; hydrogen / palladium 10% on activated carbon / ethyl acetate; ethanol / 3 h / 20 °C

4.1: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 20 °C

5.1: water; lithium hydroxide monohydrate / tetrahydrofuran; methanol / 20 °C

5.2: pH 5

With hydrogenchloride; lithium hydroxide monohydrate; hydroxylamine hydrochloride; water; hydrogen; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; palladium 10% on activated carbon; copper diacetate; In tetrahydrofuran; methanol; ethanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;

Reference yield:

: 3770-50-1,117770-52-2
2-carbethoxyindole

: 1374454-06-4
3-chloro-1-{4-[({1-[(3-methoxy-isoxazole-5-carbonyl)-amino]-cyclopropane-carbonyl}-amino)-methyl]-phenyl}-1H-indole-2-carboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: N-chloro-succinimide / acetonitrile / 20 °C / Reflux

2.1: N-ethyl-N,N-diisopropylamine / copper diacetate / N,N-dimethyl-formamide / 30 h / 20 °C / Molecular sieve

3.1: hydroxylamine hydrochloride; triethylamine / ethanol / 1 h / 20 °C

4.1: hydrogenchloride; hydrogen / palladium 10% on activated carbon / ethyl acetate; ethanol / 3 h / 20 °C

5.1: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 20 °C

6.1: water; lithium hydroxide monohydrate / tetrahydrofuran; methanol / 20 °C

6.2: pH 5

With hydrogenchloride; N-chloro-succinimide; lithium hydroxide monohydrate; hydroxylamine hydrochloride; water; hydrogen; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; palladium 10% on activated carbon; copper diacetate; In tetrahydrofuran; methanol; ethanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; acetonitrile;