Heptanoic acid, 3-[[(S)-(4-methylphenyl)sulfinyl]amino]-7-[[(4-methylphenyl)sulfonyl]oxy]-2 -[[(phenylmethoxy)carbonyl]amino]-, methyl ester, (2S,3R)-

Base Information

Chemical Name:Heptanoic acid, 3-[[(S)-(4-methylphenyl)sulfinyl]amino]-7-[[(4-methylphenyl)sulfonyl]oxy]-2 -[[(phenylmethoxy)carbonyl]amino]-, methyl ester, (2S,3R)-
CAS No.:675125-01-6
Molecular Formula:C30H36N2O8S2
Molecular Weight:616.756
Hs Code.:

Heptanoic acid,
3-[[(S)-(4-methylphenyl)sulfinyl]amino]-7-[[(4-methylphenyl)sulfonyl]oxy]-2
-[[(phenylmethoxy)carbonyl]amino]-, methyl ester, (2S,3R)-

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Heptanoic acid, 3-[[(S)-(4-methylphenyl)sulfinyl]amino]-7-[[(4-methylphenyl)sulfonyl]oxy]-2 -[[(phenylmethoxy)carbonyl]amino]-, methyl ester, (2S,3R)-

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Technology Process of Heptanoic acid, 3-[[(S)-(4-methylphenyl)sulfinyl]amino]-7-[[(4-methylphenyl)sulfonyl]oxy]-2 -[[(phenylmethoxy)carbonyl]amino]-, methyl ester, (2S,3R)-

There total 2 articles about Heptanoic acid, 3-[[(S)-(4-methylphenyl)sulfinyl]amino]-7-[[(4-methylphenyl)sulfonyl]oxy]-2 -[[(phenylmethoxy)carbonyl]amino]-, methyl ester, (2S,3R)- 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: 81.0%

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

: 675124-88-6
(+)-[(5R,6S,Ss)-6-amino-6-(methoxycarbonyl)-5-(p-tolylsulfinylamino)]hexyl p-tolylsulfonate

: 675125-01-6
(+)-[(5R,6S,Ss)-6-benzyloxycarbonylamino-6-(methoxycarbonyl)-5-(p-tolylsulfinylamino)]hexyl p-tolylsulfonate

Guidance literature:: With sodium hydroxide; In dichloromethane; water; at 0 - 20 ℃; for 4h;
DOI:10.1021/jo035613j

Reference yield:

: (+)-methyl [(2S,4R,5S,Ss)-2-phenyl-1-(p-tolylsulfinyl)-5-[4-(toluenesulfonyloxy)butyl]-1,3-imidazolidin-4-yl]carboxylate

: 675125-01-6
(+)-[(5R,6S,Ss)-6-benzyloxycarbonylamino-6-(methoxycarbonyl)-5-(p-tolylsulfinylamino)]hexyl p-tolylsulfonate

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / H₃PO₄ / tetrahydrofuran; H₂O / 4.5 h / 0 - 20 °C

2: 81 percent / NaOH / CH₂Cl₂; H₂O / 4 h / 0 - 20 °C

With sodium hydroxide; phosphoric acid; In tetrahydrofuran; dichloromethane; water;
DOI:10.1021/jo035613j