3-fluoro-1-(phenylmethoxycarbonylamino)-4-(1H-1,2,4-triazol-1-yl)benzene

Base Information

Chemical Name:3-fluoro-1-(phenylmethoxycarbonylamino)-4-(1H-1,2,4-triazol-1-yl)benzene
CAS No.:181997-14-8
Molecular Formula:C₁₆H₁₃FN₄O₂
Molecular Weight:312.303
Hs Code.:

Synonyms:3-fluoro-1-(phenylmethoxycarbonylamino)-4-(1H-1,2,4-triazol-1-yl)benzene

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Chemical Property of 3-fluoro-1-(phenylmethoxycarbonylamino)-4-(1H-1,2,4-triazol-1-yl)benzene

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Technology Process of 3-fluoro-1-(phenylmethoxycarbonylamino)-4-(1H-1,2,4-triazol-1-yl)benzene

There total 4 articles about 3-fluoro-1-(phenylmethoxycarbonylamino)-4-(1H-1,2,4-triazol-1-yl)benzene 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:

: 501-53-1,94274-21-2
benzyl chloroformate

: 181997-14-8
3-fluoro-1-(phenylmethoxycarbonylamino)-4-(1H-1,2,4-triazol-1-yl)benzene

Guidance literature:: With sodium hydrogencarbonate; In water; acetone;

Reference yield:

: 369-34-6
3,4-difluoronitrobenzene

: 181997-14-8
3-fluoro-1-(phenylmethoxycarbonylamino)-4-(1H-1,2,4-triazol-1-yl)benzene

Guidance literature:: Multi-step reaction with 3 steps

1: 72 percent / K₂HPO₄ / dimethylsulfoxide / 18 h / 90 °C

2: H₂ / Pd/C / tetrahydrofuran / 18 h / 2327.23 Torr

3: 2.6 g / NaHCO₃ / tetrahydrofuran / 48 h / -20 - 20 °C

With dipotassium hydrogenphosphate; hydrogen; sodium hydrogencarbonate; palladium on activated charcoal; In tetrahydrofuran; dimethyl sulfoxide; 1: Substitution / 2: Reduction / 3: Acylation;
DOI:10.1021/jm990373e

Reference yield:

: 182060-01-1
3-fluoro-1-nitro-4-(1H-1,2,4-triazol-1-yl)benzene

: 181997-14-8
3-fluoro-1-(phenylmethoxycarbonylamino)-4-(1H-1,2,4-triazol-1-yl)benzene

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / Pd/C / tetrahydrofuran / 18 h / 2327.23 Torr

2: 2.6 g / NaHCO₃ / tetrahydrofuran / 48 h / -20 - 20 °C

With hydrogen; sodium hydrogencarbonate; palladium on activated charcoal; In tetrahydrofuran; 1: Reduction / 2: Acylation;
DOI:10.1021/jm990373e