SK115396A3 - Regiospecific processes to make cis-1-amino-2-alkanols - Google Patents

Regiospecific processes to make cis-1-amino-2-alkanols Download PDF

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Publication number
SK115396A3
SK115396A3 SK1153-96A SK115396A SK115396A3 SK 115396 A3 SK115396 A3 SK 115396A3 SK 115396 A SK115396 A SK 115396A SK 115396 A3 SK115396 A3 SK 115396A3
Authority
SK
Slovakia
Prior art keywords
indanol
mixture
indanediol
amino
acid
Prior art date
Application number
SK1153-96A
Other languages
English (en)
Slovak (sk)
Inventor
Thomas R Verhoeven
Edward F Roberts
Chris H Senanayake
Kenneth M Ryan
Original Assignee
Merck & Co Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Merck & Co Inc filed Critical Merck & Co Inc
Publication of SK115396A3 publication Critical patent/SK115396A3/sk

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
    • C07C213/02—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton by reactions involving the formation of amino groups from compounds containing hydroxy groups or etherified or esterified hydroxy groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2602/00—Systems containing two condensed rings
    • C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
    • C07C2602/04—One of the condensed rings being a six-membered aromatic ring
    • C07C2602/08—One of the condensed rings being a six-membered aromatic ring the other ring being five-membered, e.g. indane

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
SK1153-96A 1994-03-11 1995-03-07 Regiospecific processes to make cis-1-amino-2-alkanols SK115396A3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US08/212,604 US5449830A (en) 1994-03-11 1994-03-11 Regiospecific processes to make CIS-1-Amino-2-Alkanol from Diol or Halohydrin
PCT/US1995/002830 WO1995024374A1 (en) 1994-03-11 1995-03-07 Regiospecific processes to make cis-1-amino-2-alkanol from diol or halohydrin

Publications (1)

Publication Number Publication Date
SK115396A3 true SK115396A3 (en) 1997-05-07

Family

ID=22791719

Family Applications (1)

Application Number Title Priority Date Filing Date
SK1153-96A SK115396A3 (en) 1994-03-11 1995-03-07 Regiospecific processes to make cis-1-amino-2-alkanols

Country Status (13)

Country Link
US (2) US5449830A (zh)
EP (1) EP0749410A1 (zh)
JP (1) JPH09510205A (zh)
CN (1) CN1077881C (zh)
AU (1) AU1982195A (zh)
BR (1) BR9507031A (zh)
CA (1) CA2184257A1 (zh)
CZ (1) CZ266196A3 (zh)
FI (1) FI963561A0 (zh)
RO (1) RO118425B1 (zh)
SK (1) SK115396A3 (zh)
TW (1) TW328072B (zh)
WO (1) WO1995024374A1 (zh)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5648534A (en) * 1993-12-01 1997-07-15 Ichikawa Gosei Chemical Co., Ltd. Method of producing cis-1-aminoindan-2-ol
US5618937A (en) * 1995-03-15 1997-04-08 Merck & Co., Inc. Process to make HIV protease inhibitor from (2S)-4-picolyl-2-piperazine-t-butylcarboxamide
US5824540A (en) * 1995-06-20 1998-10-20 Merck & Co., Inc. Pseudomonas putida strain with dioxygenase activity
US5858737A (en) * 1995-06-20 1999-01-12 Merck & Co., Inc. Conversion of indene to (1S)-amino-(2R)-indanol free of any stereoisomer, by combination of dioxygenase bioconversion and chemical steps
WO1998006865A1 (en) * 1996-08-14 1998-02-19 Merck & Co., Inc. Conversion of indene to (1s)-amino-(2r)-indanol free of any stereoisomer, by combination of monooxygenase bioconversion and chemical steps
US5871981A (en) * 1996-08-14 1999-02-16 Merck & Co., Inc. Conversion of indene to (1S)-amino-(2R)-indanol free of any steroisomer by combination of fermentation of Rhodococcus sp. ATCC 55805 and chemical steps
NL1006305C2 (nl) * 1997-06-13 1998-12-15 Dsm Nv Werkwijze voor de bereiding van (1S,2R)-1-amino-2-indanol-(R,R)-tartraat methanol solvaat.
CN106478429B (zh) * 2016-10-11 2018-02-13 上海瀚鸿科技股份有限公司 一种合成手性反式茚胺醇的方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1187017A (en) * 1966-07-16 1970-04-08 Aspro Nicholas Ltd Substituted 1-Amino Indanes and Tetrahydronaphthalens
US3960962A (en) * 1974-05-31 1976-06-01 Ethyl Corporation Process for replacing the hydroxy group of an aromatic hydroxy compound with an amine group
DE2658401A1 (de) * 1976-12-23 1978-07-06 Merck Patent Gmbh Cyclopentan-1-amine, verfahren zu ihrer herstellung und diese verbindungen enthaltende mittel
US4128666A (en) * 1977-08-18 1978-12-05 Smithkline Corporation 4 AND 5-Halo substituted 2-indanamine compounds
US5113025A (en) * 1989-10-02 1992-05-12 Ethyl Corporation Selective reducing agents
SG52731A1 (en) * 1991-11-08 1998-09-28 Merck & Co Inc Hiv protease inhibitors useful for the treatment of aids

Also Published As

Publication number Publication date
EP0749410A1 (en) 1996-12-27
FI963561A (fi) 1996-09-10
WO1995024374A1 (en) 1995-09-14
BR9507031A (pt) 1997-09-23
FI963561A0 (fi) 1996-09-10
AU1982195A (en) 1995-09-25
TW328072B (en) 1998-03-11
JPH09510205A (ja) 1997-10-14
CZ266196A3 (cs) 1998-02-18
RO118425B1 (ro) 2003-05-30
US5449830A (en) 1995-09-12
CN1147244A (zh) 1997-04-09
US5489710A (en) 1996-02-06
CA2184257A1 (en) 1995-09-14
CN1077881C (zh) 2002-01-16

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