(6S,7S)-6-methyl-2-phenyl-5-(phenylsulfonyl)-4,5,6,7-tetrahydro[1,3]oxazolo[4,5-c]pyridin-7-yl benzoate

Base Information

Chemical Name:(6S,7S)-6-methyl-2-phenyl-5-(phenylsulfonyl)-4,5,6,7-tetrahydro[1,3]oxazolo[4,5-c]pyridin-7-yl benzoate
CAS No.:436844-15-4
Molecular Formula:C₂₆H₂₂N₂O₅S
Molecular Weight:474.537
Hs Code.:

Synonyms:(6S,7S)-6-methyl-2-phenyl-5-(phenylsulfonyl)-4,5,6,7-tetrahydro[1,3]oxazolo[4,5-c]pyridin-7-yl benzoate

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Chemical Property of (6S,7S)-6-methyl-2-phenyl-5-(phenylsulfonyl)-4,5,6,7-tetrahydro[1,3]oxazolo[4,5-c]pyridin-7-yl benzoate

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Technology Process of (6S,7S)-6-methyl-2-phenyl-5-(phenylsulfonyl)-4,5,6,7-tetrahydro[1,3]oxazolo[4,5-c]pyridin-7-yl benzoate

There total 5 articles about (6S,7S)-6-methyl-2-phenyl-5-(phenylsulfonyl)-4,5,6,7-tetrahydro[1,3]oxazolo[4,5-c]pyridin-7-yl benzoate 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: 98.0%

: 65-85-0,8013-63-6
benzoic acid

: 221454-92-8
(6S,7R)-5-Benzenesulfonyl-6-methyl-2-phenyl-4,5,6,7-tetrahydro-oxazolo[4,5-c]pyridin-7-ol

: 436844-15-4
(6S,7S)-6-methyl-2-phenyl-5-(phenylsulfonyl)-4,5,6,7-tetrahydro[1,3]oxazolo[4,5-c]pyridin-7-yl benzoate

Guidance literature:: With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; at 0 ℃; for 15h;
DOI:10.1021/jo010665z

Reference yield:

: 101085-25-0
5-bromo-4-(bromomethyl)-2-phenyl-1,3-oxazole

: 436844-15-4
(6S,7S)-6-methyl-2-phenyl-5-(phenylsulfonyl)-4,5,6,7-tetrahydro[1,3]oxazolo[4,5-c]pyridin-7-yl benzoate

Guidance literature:: Multi-step reaction with 4 steps

1: 90 percent / K₂CO₃ / acetonitrile / 2 h / Heating

2: 74 percent / n-BuLi / hexane; tetrahydrofuran / -100 °C

3: 93 percent / NaBH₄ / tetrahydrofuran; ethanol / 2 h / 20 °C

4: 98 percent / PPh₃; DEAD / tetrahydrofuran / 15 h / 0 °C

With sodium tetrahydroborate; n-butyllithium; potassium carbonate; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; ethanol; hexane; acetonitrile; 4: Mitsunobu reaction;
DOI:10.1021/jo010665z

Reference yield:

: 59724-68-4
N-phenylsulfonyl-L-alanine methyl ester

: 436844-15-4
(6S,7S)-6-methyl-2-phenyl-5-(phenylsulfonyl)-4,5,6,7-tetrahydro[1,3]oxazolo[4,5-c]pyridin-7-yl benzoate

Guidance literature:: Multi-step reaction with 4 steps

1: 90 percent / K₂CO₃ / acetonitrile / 2 h / Heating

2: 74 percent / n-BuLi / hexane; tetrahydrofuran / -100 °C

3: 93 percent / NaBH₄ / tetrahydrofuran; ethanol / 2 h / 20 °C

4: 98 percent / PPh₃; DEAD / tetrahydrofuran / 15 h / 0 °C

With sodium tetrahydroborate; n-butyllithium; potassium carbonate; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; ethanol; hexane; acetonitrile; 4: Mitsunobu reaction;
DOI:10.1021/jo010665z