5-Hydroxymethyl-2-[(4R,4'S,4''S)-4,4',4''-trimethyl-2''-((E)-styryl)-4,5,4',5',4'',5''-hexahydro-[2,4';2',4'']terthiazol-4-yl]-oxazole-4-carboxylic acid methylamide

Base Information

Chemical Name:5-Hydroxymethyl-2-[(4R,4'S,4''S)-4,4',4''-trimethyl-2''-((E)-styryl)-4,5,4',5',4'',5''-hexahydro-[2,4';2',4'']terthiazol-4-yl]-oxazole-4-carboxylic acid methylamide
CAS No.:257278-45-8
Molecular Formula:C₂₆H₂₉N₅O₃S₃
Molecular Weight:555.746
Hs Code.:

Synonyms:5-Hydroxymethyl-2-[(4R,4'S,4''S)-4,4',4''-trimethyl-2''-((E)-styryl)-4,5,4',5',4'',5''-hexahydro-[2,4';2',4'']terthiazol-4-yl]-oxazole-4-carboxylic acid methylamide

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Chemical Property of 5-Hydroxymethyl-2-[(4R,4'S,4''S)-4,4',4''-trimethyl-2''-((E)-styryl)-4,5,4',5',4'',5''-hexahydro-[2,4';2',4'']terthiazol-4-yl]-oxazole-4-carboxylic acid methylamide

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Technology Process of 5-Hydroxymethyl-2-[(4R,4'S,4''S)-4,4',4''-trimethyl-2''-((E)-styryl)-4,5,4',5',4'',5''-hexahydro-[2,4';2',4'']terthiazol-4-yl]-oxazole-4-carboxylic acid methylamide

There total 3 articles about 5-Hydroxymethyl-2-[(4R,4'S,4''S)-4,4',4''-trimethyl-2''-((E)-styryl)-4,5,4',5',4'',5''-hexahydro-[2,4';2',4'']terthiazol-4-yl]-oxazole-4-carboxylic acid methylamide 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: 68.0%

: 138667-71-7,144370-38-7
(-)-Thiangazole

: angabazole

: 5-desmethylthiangazole

: 257278-45-8
5-Hydroxymethyl-2-[(4R,4'S,4''S)-4,4',4''-trimethyl-2''-((E)-styryl)-4,5,4',5',4'',5''-hexahydro-[2,4';2',4'']terthiazol-4-yl]-oxazole-4-carboxylic acid methylamide

Guidance literature:: With potassium tert-butylate; oxygen; In dimethyl sulfoxide; at 20 ℃; for 0.5h;
DOI:10.1002/(SICI)1099-0690(199912)1999:12<3381::AID-EJOC3381>3.0.CO;2-W

Reference yield:

: 1100-88-5
benzyltriphenylphosphonium chloride

: 257278-45-8
5-Hydroxymethyl-2-[(4R,4'S,4''S)-4,4',4''-trimethyl-2''-((E)-styryl)-4,5,4',5',4'',5''-hexahydro-[2,4';2',4'']terthiazol-4-yl]-oxazole-4-carboxylic acid methylamide

Guidance literature:: Multi-step reaction with 2 steps

1: 36 percent / 50 percent NaOH / H₂O; CH₂Cl₂ / 0.5 h / 20 °C

2: 68 percent / O₂; KOtBu / dimethylsulfoxide / 0.5 h / 20 °C

With sodium hydroxide; potassium tert-butylate; oxygen; In dichloromethane; water; dimethyl sulfoxide; 1: Wittig reaction / 2: Oxidation;
DOI:10.1002/(SICI)1099-0690(199912)1999:12<3381::AID-EJOC3381>3.0.CO;2-W

Reference yield:

: 257278-51-6
2-((4R,4'S,4''S)-2''-Formyl-4,4',4''-trimethyl-4,5,4',5',4'',5''-hexahydro-[2,4';2',4'']terthiazol-4-yl)-5-methyl-oxazole-4-carboxylic acid methylamide

: 257278-45-8
5-Hydroxymethyl-2-[(4R,4'S,4''S)-4,4',4''-trimethyl-2''-((E)-styryl)-4,5,4',5',4'',5''-hexahydro-[2,4';2',4'']terthiazol-4-yl]-oxazole-4-carboxylic acid methylamide

Guidance literature:: Multi-step reaction with 2 steps

1: 36 percent / 50 percent NaOH / H₂O; CH₂Cl₂ / 0.5 h / 20 °C

2: 68 percent / O₂; KOtBu / dimethylsulfoxide / 0.5 h / 20 °C

With sodium hydroxide; potassium tert-butylate; oxygen; In dichloromethane; water; dimethyl sulfoxide; 1: Wittig reaction / 2: Oxidation;
DOI:10.1002/(SICI)1099-0690(199912)1999:12<3381::AID-EJOC3381>3.0.CO;2-W