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CAS号57728-40-2 2-氨基-3-甲基-1,1-二... | CAS号223906-36-3 (2R)-N-B°C-2-am... | CAS号106391-85-9 甲基N-{[(2-甲基-2-丙...合成工艺路线路线简述
- 合成目标产物 (R)-(+)-2-Amino-3-Methyl-1,1-Diphenyl-1-Butanol 主要起始原料 (R)-Tert-Butyl 1-Hydroxy-3-Methyl-1,1-Diphenylbutan-2-Ylcarbamate
- (文献来源)合成步骤主要原料 (R)-Tert-Butyl 1-Hydroxy-3-Methyl-1,1-Diphenylbutan-2-Ylcarbamate
甲基n-{[(2-甲基-2-丙基)氧基]羰基}-D-缬氨酸酯置于盐酸,甲醇体系中,用 乙醚 作为反应溶剂,化学反应 4.0H,反应生成 (R)-(+)-2-氨基-3-甲基-1,1-二苯基-1-丁醇
参考文献:Diastereoselective Reduction Of A Chiral N-Boc-Protected δ-Amino-α,β-Unsaturated γ-Keto Ester Phe-Gly Dipeptidomimetic
标题:Diastereoselective Reduction Of A Chiral N-Boc-Protected δ-Amino-α,β-Unsaturated γ-Keto Ester Phe-Gly Dipeptidomimetic
摘要:The Readily Available N-Boc-Protected Delta-Amino Alpha,Beta-Unsaturated Gamma-Keto Ester 1 Was Diastereoselectively Reduced To The Corresponding Alcohols 2 And 3,Using Boron-And Aluminum-Based Reducing Reagents. Reduction Reactions Were Successful And Resulted In Anti/syn Ratios Of Alcohols Of >95:5 (80% Yield),Using Lialh(O-T-Bu)(3) In Etoh At-78Degreesc Under Chelation Control,And 5:95 (98% Yield),Using Nb-Enantride In Thf At-78Degreesc Under Felkin-Anh Control.
DOI:10.1021/jo020442O
海关参考信息
- 2902600000-乙苯
2905121000-正丙醇
2905130000-正丁醇
2906210000-苄醇 - 💡 提示:海关信息按照顺序优先匹配,如需确认的海关信息,请参考相关资料。
- 详情请参考:📖 海关编码查询和海关进出口税则
专利信息
专利号:EP-1730108-B1
优先权日:2004-03-18
标 题:Stereoselective synthesis of vitamin d analogues
发明人:SABROE THOMAS PETER; CALVERLEY MARTIN JOHN
权利人:LEO PHARMA AS
摘要:The present invention relates to intermediates useful for the synthesis of calcipotriol or calcipotriol monohydrate, to methods of producing said intermediates, and to methods of stereoselectively reducing said intermediates.
专利号:EP-1735276-B1
优先权日:2004-04-02
标题:Novel method for the preparation of intermediates useful for the synthesis of vitamin d analogues
发明人:HANSEN ERIK TORNGAARD; SABROE THOMAS PETER; CALVERLEY MARTIN JOHN; PEDERSEN HENRIK; DEUSSEN HEINZ-JOSEF WILHELM
权利人:LEO PHARMA AS
摘要:The present invention relates to novel methods for the preparation of intermediates which are useful in the synthesis of cacipotriol. The present invention relates further to the use of intermediates produced with said methods for making calcipotriol or calcipotriol monohydrate.
专利号:US-8759555-B2
优先权日:2004-03-18
标 题:Stereoselective synthesis of vitamin D analogues
发明人:SABROE THOMAS PETER; CALVERLEY MARTIN JOHN
权利人:SABROE THOMAS PETER; CALVERLEY MARTIN JOHN; LEO PHARMA AS
摘要:The present invention relates to intermediates useful for the synthesis of calcipotriol or calcipotriol monohydrate, to methods of producing said intermediates, and to methods of stereoselectively reducing said intermediates.
专利号:RU-2378252-C2
优先权日:2004-04-02
标题 :Novel method for synthesis of intermediate compounds, used in synthesis of vitamin d analogues
专利号:WO-9501357-A1
优先权日:1993-07-02
标题 :Optically active 1-(4-nitrophenyl)-4-methyl-7,8-methylenedioxy-3,4-dihydro-5h-2,3-benzodiazepine and process for preparing same
发明人:LING ISTVAN; HAMORI TAMAS; BOTKA PETER; SOLYOM SANDOR; SIMAY ANTAL; MORAVCSIK IMRE
权利人:GYOGYSZERKUTATO INTEZET; LING ISTVAN; HAMORI TAMAS; BOTKA PETER; SOLYOM SANDOR; SIMAY ANTAL; MORAVCSIK IMRE
摘要:The invention relates to the (+)- and (-)-enantiomers of the compounds of formula (I) as well as a process for the preparation of these enantiomers. This process comprises reducing 1-(4-nitrophenyl)-4-methyl-7,8-methylenedioxy-5H^_-2,3-benzodiazepine of formula (II) by using an adduct formed from an (R)- or (S)-, respectively, 2-amino-1,1-diphenyl-alkan-1-ol derivative of general formula (III), wherein R1 and R2, which are different, stand for a straight or branched chain C1-4 alkyl group or an unsubstituted phenyl or benzyl group, with one molar equivalent of borane or a borane complex. The enantiomers of the compound of formula (I) are valuable intermediates in the synthesis of therapeutically active compounds.
专利号:US-2007027333-A1
优先权日:2004-03-18
标题 :Stereoselective synthesis of vitamin d analogues