WO2008078563A1 - 3-ベンジルオキシベンゼンチオールの製造方法 - Google Patents
3-ベンジルオキシベンゼンチオールの製造方法 Download PDFInfo
- Publication number
- WO2008078563A1 WO2008078563A1 PCT/JP2007/074001 JP2007074001W WO2008078563A1 WO 2008078563 A1 WO2008078563 A1 WO 2008078563A1 JP 2007074001 W JP2007074001 W JP 2007074001W WO 2008078563 A1 WO2008078563 A1 WO 2008078563A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- benzyloxybenzenethiol
- production
- reacting
- general formula
- grignard reagent
- Prior art date
- Legal status (The legal status 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 status listed.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B49/00—Grignard reactions
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C319/00—Preparation of thiols, sulfides, hydropolysulfides or polysulfides
- C07C319/02—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of thiols
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
本発明は、一般式(1); (式中、Xはハロゲン原子を示す。)で表される3-ベンジルオキシハロベンゼンと金属マグネシウムとを反応させて一般式(2); (式中、Xは前記と同様である。)で表されるグリニャール試薬となし、このグリニャール試薬と硫黄とを反応させることを特徴とする式(3); で表される3-ベンジルオキシベンゼンチオールの製造方法を提供する。
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2008551029A JP5153648B2 (ja) | 2006-12-22 | 2007-12-13 | 3−ベンジルオキシベンゼンチオールの製造方法 |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2006-345382 | 2006-12-22 | ||
| JP2006345382 | 2006-12-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2008078563A1 true WO2008078563A1 (ja) | 2008-07-03 |
Family
ID=39562357
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2007/074001 Ceased WO2008078563A1 (ja) | 2006-12-22 | 2007-12-13 | 3-ベンジルオキシベンゼンチオールの製造方法 |
Country Status (2)
| Country | Link |
|---|---|
| JP (1) | JP5153648B2 (ja) |
| WO (1) | WO2008078563A1 (ja) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012073249A1 (en) | 2010-12-01 | 2012-06-07 | Arch Pharmalabs Limited | A novel process for the preparation of 3-(benzyloxy)- benzenethiol, a key intermediate for the preparation of pharmaceutical drugs. |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005087731A1 (en) * | 2004-02-27 | 2005-09-22 | Schering Corporation | Sulfur compounds as inhibitors of hepatitis c virus ns3 serine protease |
| WO2006041019A1 (ja) * | 2004-10-12 | 2006-04-20 | Kyorin Pharmaceutical Co., Ltd. | 2-アミノ-2-[2-[4-(3-ベンジルオキシフェニルチオ)-2-クロロフェニル]エチル]-1,3-プロパンジオール塩酸塩又はその水和物の製造方法及びその製造中間体 |
-
2007
- 2007-12-13 JP JP2008551029A patent/JP5153648B2/ja not_active Expired - Fee Related
- 2007-12-13 WO PCT/JP2007/074001 patent/WO2008078563A1/ja not_active Ceased
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005087731A1 (en) * | 2004-02-27 | 2005-09-22 | Schering Corporation | Sulfur compounds as inhibitors of hepatitis c virus ns3 serine protease |
| WO2006041019A1 (ja) * | 2004-10-12 | 2006-04-20 | Kyorin Pharmaceutical Co., Ltd. | 2-アミノ-2-[2-[4-(3-ベンジルオキシフェニルチオ)-2-クロロフェニル]エチル]-1,3-プロパンジオール塩酸塩又はその水和物の製造方法及びその製造中間体 |
Non-Patent Citations (4)
| Title |
|---|
| HIROYUKI K. ET AL.: "Convenient Route to Fischer-Type Carbene Ruthenium Complexes: Highly Selective Catalysts for Ring Opening/Cross-Metathesis of Norbornene Derivatives", ORGANOMETALLICS, vol. 22, 2003, pages 586 - 593, XP001141875, DOI: doi:10.1021/om020772z * |
| JIANJI W. ET AL.: "Highly convergent synthesis of a rebeccamycin analog with benzothioeno (2,3-a)pyrrolo(3,4-c)carbazole as the aglycone", TETRAHEDRON LETTERS, vol. 46, 2005, pages 907 - 910 * |
| THOMAS P.J. ET AL.: "SYNTHESIS OF NOVEL BENZOCYCLOBUTENE COMPOUNDS", SYNTHETIC COMMUNICATIONS, vol. 25, no. 18, 1995, pages 2813 - 2817 * |
| YUKIO H. ET AL.: "Synthesis of 4-thia-2-azapodophyllooxin, a new analogue of the antitumour lignan podophyllotoxin", J. CHEM. SOC. PERKIN TRANS. 1, no. 11, 1995, pages 1387 - 1390, XP002139429 * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012073249A1 (en) | 2010-12-01 | 2012-06-07 | Arch Pharmalabs Limited | A novel process for the preparation of 3-(benzyloxy)- benzenethiol, a key intermediate for the preparation of pharmaceutical drugs. |
Also Published As
| Publication number | Publication date |
|---|---|
| JP5153648B2 (ja) | 2013-02-27 |
| JPWO2008078563A1 (ja) | 2010-04-22 |
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