(R)-4-(1-((4-(tert-butoxycarbonyl)morpholin-2-yl)methyl)-5-methyl-1H-benzo[d]imidazol-2-yl)-3,5-difluorobenzoic acid

Base Information

Chemical Name:(R)-4-(1-((4-(tert-butoxycarbonyl)morpholin-2-yl)methyl)-5-methyl-1H-benzo[d]imidazol-2-yl)-3,5-difluorobenzoic acid
CAS No.:1308849-96-8
Molecular Formula:C₂₅H₂₇F₂N₃O₅
Molecular Weight:487.503
Hs Code.:

Synonyms:(R)-4-(1-((4-(tert-butoxycarbonyl)morpholin-2-yl)methyl)-5-methyl-1H-benzo[d]imidazol-2-yl)-3,5-difluorobenzoic acid

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Chemical Property of (R)-4-(1-((4-(tert-butoxycarbonyl)morpholin-2-yl)methyl)-5-methyl-1H-benzo[d]imidazol-2-yl)-3,5-difluorobenzoic acid

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Technology Process of (R)-4-(1-((4-(tert-butoxycarbonyl)morpholin-2-yl)methyl)-5-methyl-1H-benzo[d]imidazol-2-yl)-3,5-difluorobenzoic acid

There total 6 articles about (R)-4-(1-((4-(tert-butoxycarbonyl)morpholin-2-yl)methyl)-5-methyl-1H-benzo[d]imidazol-2-yl)-3,5-difluorobenzoic 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: 82.0%

: 736990-88-8
3,5-difluoro-4-formylbenzoic acid

: 1308849-95-7
(R)-tert-butyl 2-((2-amino-4-methylphenylamino)methyl)morpholine-4-carboxylate

: 1308849-96-8
(R)-4-(1-((4-(tert-butoxycarbonyl)morpholin-2-yl)methyl)-5-methyl-1H-benzo[d]imidazol-2-yl)-3,5-difluorobenzoic acid

Guidance literature:: With acetic acid; In methanol; at 20 ℃; for 1.5h;

Reference yield:

: 455-40-3
3,5-difluorobenzoic acid

: 1308849-96-8
(R)-4-(1-((4-(tert-butoxycarbonyl)morpholin-2-yl)methyl)-5-methyl-1H-benzo[d]imidazol-2-yl)-3,5-difluorobenzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: N,N,N,N,-tetramethylethylenediamine / 2-methyltetrahydrofuran / 20 °C

1.2: 1.5 h / -78 - -65 °C

2.1: acetic acid / methanol / 1.5 h / 20 °C

With N,N,N,N,-tetramethylethylenediamine; acetic acid; In 2-methyltetrahydrofuran; methanol;

Reference yield:

: 606139-90-6
tert-butyl (2S)-2-{[(methylsulfonyl)oxy]methyl}morpholine-4-carboxylate

: 1308849-96-8
(R)-4-(1-((4-(tert-butoxycarbonyl)morpholin-2-yl)methyl)-5-methyl-1H-benzo[d]imidazol-2-yl)-3,5-difluorobenzoic acid

Guidance literature:: Multi-step reaction with 5 steps

1: N,N-dimethyl-formamide / 16 h / 110 - 115 °C

2: ethanolamine / 16 h / 20 °C

3: N-ethyl-N,N-diisopropylamine / methanol / 0.5 h / 140 °C / microwave irradiation

4: zinc; acetic acid / methanol / 90 h / 20 °C

5: acetic acid / methanol / 1.5 h / 20 °C

With ethanolamine; acetic acid; N-ethyl-N,N-diisopropylamine; zinc; In methanol; N,N-dimethyl-formamide;