dl-(1β,2α,3β,5β)-2-(hydroxyethyl)-3-<(phenylsulfonyl)amino>bicyclo<3.1.0>hexane

Base Information

Chemical Name:dl-(1β,2α,3β,5β)-2-(hydroxyethyl)-3-<(phenylsulfonyl)amino>bicyclo<3.1.0>hexane
CAS No.:112917-40-5
Molecular Formula:C₁₄H₁₉NO₃S
Molecular Weight:281.376
Hs Code.:

Synonyms:dl-(1β,2α,3β,5β)-2-(hydroxyethyl)-3-<(phenylsulfonyl)amino>bicyclo<3.1.0>hexane

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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 dl-(1β,2α,3β,5β)-2-(hydroxyethyl)-3-<(phenylsulfonyl)amino>bicyclo<3.1.0>hexane

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Technology Process of dl-(1β,2α,3β,5β)-2-(hydroxyethyl)-3-<(phenylsulfonyl)amino>bicyclo<3.1.0>hexane

There total 6 articles about dl-(1β,2α,3β,5β)-2-(hydroxyethyl)-3-<(phenylsulfonyl)amino>bicyclo<3.1.0>hexane 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: 16.0%

: 112917-38-1,112917-39-2,112917-42-7
N-[(1S,2S,5S)-2-(2-Trityloxy-ethyl)-bicyclo[3.1.0]hex-3-yl]-benzenesulfonamide

: 112917-40-5
dl-(1β,2α,3β,5β)-2-(hydroxyethyl)-3-<(phenylsulfonyl)amino>bicyclo<3.1.0>hexane

: 112917-34-7
dl-(1β,2α,3α,5β)-2-(hydroxyethyl)-3-<(phenylsulfonyl)amino>bicyclo<3.1.0>hexane

Guidance literature:: With acetic acid; for 15h; Heating;
DOI:10.1021/jm00163a038

Reference yield:

: 112918-24-8
dl-(1β,2α,3α,5β)-2-(hydroxyethyl)-3-hydroxybicyclo<3.1.0>hexane

: 112917-40-5
dl-(1β,2α,3β,5β)-2-(hydroxyethyl)-3-<(phenylsulfonyl)amino>bicyclo<3.1.0>hexane

Guidance literature:: Multi-step reaction with 6 steps

1: 95.7 percent / Et₃N, 4-(dimethylamino)pyridine / CH₂Cl₂ / 1.) 0 deg C, 30 min, 2.) RT, 20 h

2: 56.8 percent / PDC / dimethylformamide / 3 h / Ambient temperature

3: 99 percent / KOH, NH₂OH*HCl / methanol / 3 h / Ambient temperature

4: 1.) diphenyl disulfide, n-Bu₃P, 2.) sodium cyanoborohydride, acetic acid / 1.) THF, RT, 1 h, 2.) -70 deg C, 10 min

5: 2.18 g / Et₃N / CH₂Cl₂ / 3 h / Ambient temperature

6: 63 percent / 80percent aq. AcOH / 15 h / Heating

With dmap; potassium hydroxide; dipyridinium dichromate; tributylphosphine; hydroxylamine hydrochloride; sodium cyanoborohydride; acetic acid; triethylamine; diphenyldisulfane; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm00163a038

Reference yield:

: 123490-00-6,123490-01-7,123490-02-8
(1S,2S,5S)-2-(2-Trityloxy-ethyl)-bicyclo[3.1.0]hex-3-ylamine

: 112917-40-5
dl-(1β,2α,3β,5β)-2-(hydroxyethyl)-3-<(phenylsulfonyl)amino>bicyclo<3.1.0>hexane

Guidance literature:: Multi-step reaction with 2 steps

1: 2.18 g / Et₃N / CH₂Cl₂ / 3 h / Ambient temperature

2: 63 percent / 80percent aq. AcOH / 15 h / Heating

With acetic acid; triethylamine; In dichloromethane;
DOI:10.1021/jm00163a038