(1R,2S)-2-(tert-butyloxycarbonylamino)-1-<1-(phenylsulfonyl)-2-indolyl>-1,3-propanediol

Base Information

Chemical Name:(1R,2S)-2-(tert-butyloxycarbonylamino)-1-<1-(phenylsulfonyl)-2-indolyl>-1,3-propanediol
CAS No.:152706-29-1
Molecular Formula:C₂₂H₂₆N₂O₆S
Molecular Weight:446.524
Hs Code.:

Synonyms:(1R,2S)-2-(tert-butyloxycarbonylamino)-1-<1-(phenylsulfonyl)-2-indolyl>-1,3-propanediol

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Chemical Property of (1R,2S)-2-(tert-butyloxycarbonylamino)-1-<1-(phenylsulfonyl)-2-indolyl>-1,3-propanediol

Chemical Property:

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Technology Process of (1R,2S)-2-(tert-butyloxycarbonylamino)-1-<1-(phenylsulfonyl)-2-indolyl>-1,3-propanediol

There total 3 articles about (1R,2S)-2-(tert-butyloxycarbonylamino)-1-<1-(phenylsulfonyl)-2-indolyl>-1,3-propanediol 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: 90.0%

: 152706-53-1
tert-butyl (4S)-2,2-dimethyl-4-<(R)-hydroxyl<1-(phenylsulfonyl)-2-indolyl>methyl>-3-oxazolidinecarboxylate

: 152706-29-1
(1R,2S)-2-(tert-butyloxycarbonylamino)-1-<1-(phenylsulfonyl)-2-indolyl>-1,3-propanediol

Guidance literature:: With hydrogenchloride; In methanol; for 1h; Ambient temperature;
DOI:10.1248/cpb.41.854

Reference yield:

: 40899-71-6
1-benzenesulfonylindole

: 152706-29-1
(1R,2S)-2-(tert-butyloxycarbonylamino)-1-<1-(phenylsulfonyl)-2-indolyl>-1,3-propanediol

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) BuLi / 1.) hexane, THF, from -88 to -82 deg C, 20 min, 2.) hexane, THF, from -88 to -75 deg C, 30 min

2: 90 percent / 10percent aq. HCl / methanol / 1 h / Ambient temperature

With hydrogenchloride; n-butyllithium; In methanol;
DOI:10.1248/cpb.41.854

Reference yield:

: 102308-32-7
(4S)-4-formyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

: 152706-29-1
(1R,2S)-2-(tert-butyloxycarbonylamino)-1-<1-(phenylsulfonyl)-2-indolyl>-1,3-propanediol

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) BuLi / 1.) hexane, THF, from -88 to -82 deg C, 20 min, 2.) hexane, THF, from -88 to -75 deg C, 30 min

2: 90 percent / 10percent aq. HCl / methanol / 1 h / Ambient temperature

With hydrogenchloride; n-butyllithium; In methanol;
DOI:10.1248/cpb.41.854