[4-(3-tert-butyl-5-{[(1,3-thiazol-2-ylamino)carbonyl]amino}-1H-pyrazol-1-yl)phenyl]acetic acid

Base Information

Chemical Name:[4-(3-tert-butyl-5-{[(1,3-thiazol-2-ylamino)carbonyl]amino}-1H-pyrazol-1-yl)phenyl]acetic acid
CAS No.:1357621-30-7
Molecular Formula:C₁₉H₂₁N₅O₃S
Molecular Weight:399.473
Hs Code.:

Synonyms:[4-(3-tert-butyl-5-{[(1,3-thiazol-2-ylamino)carbonyl]amino}-1H-pyrazol-1-yl)phenyl]acetic acid

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Chemical Property of [4-(3-tert-butyl-5-{[(1,3-thiazol-2-ylamino)carbonyl]amino}-1H-pyrazol-1-yl)phenyl]acetic acid

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Technology Process of [4-(3-tert-butyl-5-{[(1,3-thiazol-2-ylamino)carbonyl]amino}-1H-pyrazol-1-yl)phenyl]acetic acid

There total 4 articles about [4-(3-tert-butyl-5-{[(1,3-thiazol-2-ylamino)carbonyl]amino}-1H-pyrazol-1-yl)phenyl]acetic 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:

: 1357621-29-4
ethyl [4-(3-tert-butyl-5-{[(1,3-thiazol-2-ylamino)carbonyl]amino}-1H-pyrazol-1-yl)phenyl]acetate

: 1357621-30-7
[4-(3-tert-butyl-5-{[(1,3-thiazol-2-ylamino)carbonyl]amino}-1H-pyrazol-1-yl)phenyl]acetic acid

Guidance literature:: ethyl [4-(3-tert-butyl-5-{[(1,3-thiazol-2-ylamino)carbonyl]amino}-1H-pyrazol-1-yl)phenyl]acetate; With lithium hydroxide; In methanol; water; at 20 ℃; for 0.5h;

With formic acid; In methanol; water;
DOI:10.1016/j.ejmech.2011.11.019

Reference yield:

: 1357621-07-8
ethyl [4-(3-tert-butyl-5-{[(2,2,2-trichloroethoxy)carbonyl]amino}-1H-pyrazol-1-yl)phenyl]acetate

: 1357621-30-7
[4-(3-tert-butyl-5-{[(1,3-thiazol-2-ylamino)carbonyl]amino}-1H-pyrazol-1-yl)phenyl]acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 60 °C / Microwave irradiation

2: lithium hydroxide / methanol; water / 0.5 h / 20 °C

With N-ethyl-N,N-diisopropylamine; lithium hydroxide; In methanol; water; dimethyl sulfoxide;
DOI:10.1016/j.ejmech.2011.11.019

Reference yield:

: 1197-55-3
4-aminophenylacetic acid

: 1357621-30-7
[4-(3-tert-butyl-5-{[(1,3-thiazol-2-ylamino)carbonyl]amino}-1H-pyrazol-1-yl)phenyl]acetic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogenchloride; sodium nitrite / water / 1 h / 0 °C

1.2: 2 h / 0 - 20 °C

2.1: Reflux

3.1: sodium hydroxide / water; ethyl acetate / 2.5 h / 0 - 20 °C

4.1: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 60 °C / Microwave irradiation

5.1: lithium hydroxide / methanol; water / 0.5 h / 20 °C

With hydrogenchloride; N-ethyl-N,N-diisopropylamine; sodium hydroxide; lithium hydroxide; sodium nitrite; In methanol; water; dimethyl sulfoxide; ethyl acetate;
DOI:10.1016/j.ejmech.2011.11.019