KR960034212A - 5-메틸우리딘으로부터 디4티를 제조하는 방법 - Google Patents
5-메틸우리딘으로부터 디4티를 제조하는 방법 Download PDFInfo
- Publication number
- KR960034212A KR960034212A KR1019960005683A KR19960005683A KR960034212A KR 960034212 A KR960034212 A KR 960034212A KR 1019960005683 A KR1019960005683 A KR 1019960005683A KR 19960005683 A KR19960005683 A KR 19960005683A KR 960034212 A KR960034212 A KR 960034212A
- Authority
- KR
- South Korea
- Prior art keywords
- mixture
- compound
- bromo
- treating
- chloro
- Prior art date
Links
- DWRXFEITVBNRMK-UHFFFAOYSA-N Beta-D-1-Arabinofuranosylthymine Natural products O=C1NC(=O)C(C)=CN1C1C(O)C(O)C(CO)O1 DWRXFEITVBNRMK-UHFFFAOYSA-N 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- DWRXFEITVBNRMK-JXOAFFINSA-N ribothymidine Chemical compound O=C1NC(=O)C(C)=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 DWRXFEITVBNRMK-JXOAFFINSA-N 0.000 title 1
- 238000000034 method Methods 0.000 claims abstract 8
- 239000000203 mixture Substances 0.000 claims 15
- 150000001875 compounds Chemical class 0.000 claims 12
- 125000001246 bromo group Chemical group Br* 0.000 claims 8
- 150000002118 epoxides Chemical class 0.000 claims 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims 6
- 229910052751 metal Inorganic materials 0.000 claims 6
- 239000002184 metal Substances 0.000 claims 6
- XNKLLVCARDGLGL-JGVFFNPUSA-N Stavudine Chemical compound O=C1NC(=O)C(C)=CN1[C@H]1C=C[C@@H](CO)O1 XNKLLVCARDGLGL-JGVFFNPUSA-N 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 125000001309 chloro group Chemical group Cl* 0.000 claims 5
- BMFGLXWWIGPMOM-IHPAWCCZSA-N 1-[(2r,3r,4s,5r)-3,4-dihydroxy-5-[hydroxy(methylsulfonyl)methyl]-3,4-bis(methylsulfonyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione Chemical compound O=C1NC(=O)C(C)=CN1[C@H]1[C@](S(C)(=O)=O)(O)[C@@](O)(S(C)(=O)=O)[C@@H](C(O)S(C)(=O)=O)O1 BMFGLXWWIGPMOM-IHPAWCCZSA-N 0.000 claims 4
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims 4
- 150000001266 acyl halides Chemical class 0.000 claims 4
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims 4
- 229910000039 hydrogen halide Inorganic materials 0.000 claims 4
- 239000012433 hydrogen halide Substances 0.000 claims 4
- 125000002346 iodo group Chemical group I* 0.000 claims 4
- MEKOFIRRDATTAG-UHFFFAOYSA-N 2,2,5,8-tetramethyl-3,4-dihydrochromen-6-ol Chemical compound C1CC(C)(C)OC2=C1C(C)=C(O)C=C2C MEKOFIRRDATTAG-UHFFFAOYSA-N 0.000 claims 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims 3
- 229910052725 zinc Inorganic materials 0.000 claims 3
- 239000011701 zinc Substances 0.000 claims 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 2
- 150000003973 alkyl amines Chemical class 0.000 claims 2
- 239000003638 chemical reducing agent Substances 0.000 claims 2
- 229910000042 hydrogen bromide Inorganic materials 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 1
- FXXACINHVKSMDR-UHFFFAOYSA-N acetyl bromide Chemical compound CC(Br)=O FXXACINHVKSMDR-UHFFFAOYSA-N 0.000 claims 1
- 239000003513 alkali Substances 0.000 claims 1
- 150000001342 alkaline earth metals Chemical class 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- OKYMAJFPIZNKLF-UHFFFAOYSA-N bromosyl acetate Chemical group Br(=O)OC(C)=O OKYMAJFPIZNKLF-UHFFFAOYSA-N 0.000 claims 1
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 claims 1
- 229910052791 calcium Inorganic materials 0.000 claims 1
- 239000011575 calcium Substances 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims 1
- 229910052744 lithium Inorganic materials 0.000 claims 1
- 229910052749 magnesium Inorganic materials 0.000 claims 1
- 239000011777 magnesium Substances 0.000 claims 1
- 229910052700 potassium Inorganic materials 0.000 claims 1
- 239000011591 potassium Substances 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 claims 1
- 235000010234 sodium benzoate Nutrition 0.000 claims 1
- 239000004299 sodium benzoate Substances 0.000 claims 1
- 239000000543 intermediate Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
Abstract
본 발명은 5-MU로부터 d4T를 제조하는 개선된 방법에 관한다. 본 발명의 또 다른 측면은 공정 중 생산된 유용한 중간체에도 관한 것이다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (15)
- a) 2',3',5'-트리스(메탄설포닐)-5-메틸우리딘(2)를알카리 금속 수산화물로 처리하여 에폭사이드(3)을 얻고;b) 에폭사이드(3)을 할로겐화 수소를 처리하여 X가 클로로, 브로모 또는 요오도인 화합물(4a)와 (4b)의 혼합물을 얻은 다음;c) (4a)와 (4b)의 혼합물을 아실 할라이드로 처리하여 R이 C1-6알킬인 (5a)와 (5b)의 혼합물을 얻은 다음;d) (5a)와 (5b)의 혼합물을 환원 금속으로 처리하여 화합물(6)을 얻는 단계로 이루어지는 2',3'-디데히드로-3'-데옥시티미딘(d4T)의 제조방법.
- 제1항에 있어서, (a) 단계의 알칼리 금속 수산화물이 수산화나트륨인 방법.
- 제1항에 있어서, (b) 단계의 할로겐화 수소가 브롬화 수소인 방법.
- 제1항에 있어서, (c) 단계의 아실 할라이드가 아세틸 브로마이드인 방법.
- 제1항에 있어서, (d) 단계의 환원 금속이 아연인 방법.
- 화합물(5a) 또는 (5b), 또는 이들의 혼합물을(식 중, X는 클로로, 브로모 또는 요오드이고; R은 C1-6알킬임) 금속 환원제와 반응시켜 일반식(6)의 화합물을 얻는 것으로 되는, 2'.3'-디데히드로-3'-데옥시티미딘(d4T)의 제조방법.
- 제6항에 있어서, R이 메틸이고, X는 브로모이며, 금속 환원제는 아연인 방법.
- 다음 일반식(3)의 화합물.
- 화합물(4a) 또는 (4b)의 혼합물, 또는 이들의 혼합물.식 중, X는 클로로, 브로모 또는 요오도임.
- 제9항에 있어서, X가 브로모인 화합물 또는 혼합물.
- 화합물(5a) 또는 (5b)의 혼합물, 또는 이들의 혼합물.식 중, X는 클로로, 브로모 또는 요오도이고; R은 C1-6알킬임.
- 제11항에 있어서, X가 브로모이고 R은 메틸인 화합물 또는 혼합물.
- a) 2',3',5'-트리스(메탄설포닐)-5-메틸우리딘(2)를알카리 금속 수산화물로 처리하여 에폭사이드(3)을 얻고;b) 에폭사이드(3)을 할로겐화수소로 처리하여 X가 클로로, 브로모 또는 요오도인 화합물(4a) 및 (4b)의 혼합물을 얻은 다음c) (4a)와 (4b)의 혼합물을 아실 할라이드로 처리하여 R이 C1-6알킬인 (5a)와 (5b)의 혼합물을 얻은 후;d) (5a)와 (5b)의 혼합물을 환원 금속으로 처리하여 화합물(6)을 제공한 다음;e) 화합물(6)의 화합물 R'COOT(여기서 T는 나트륨, 칼륨, 리튬, 칼슘 또는 마그네슘 중에서 선택된 알칼리 또는 알칼리토 금속이고; R'은 아릴 또는 C1-6알킬임)로 처리하여 일반식(7)의 화합물을 얻고;f) 일반식(7)의 화합물 R'COO-래디칼을 C1-6알킬아민을 이용하여 히드록시로 전환시키는 단계로 이루어지는 2',3'-디데히드로-3'-데옥시티미딘(d4T)의 제조방법.
- 내용 없음
- 제14항에 있어서, (a) 단계의 알칼리 금속 수산화물이 수산화나트륨이고; (b) 단계의 할로겐화 수소는 브롬화 수소이며; (c) 단계는 아실 할라이드는 아세틸 브로마이트이고; (d) 단계의 환원 금속은 아연이며; (e) 단계의 R'COOT는 벤조산나트륨이고; (f) 단계의 C1-6알킬아민은 n-부틸아민인 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/402,283 US5608049A (en) | 1995-03-10 | 1995-03-10 | Preparation of d4T from 5-methyluridine |
US08/402,283 | 1995-03-10 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR960034212A true KR960034212A (ko) | 1996-10-22 |
KR100393913B1 KR100393913B1 (ko) | 2003-12-18 |
Family
ID=23591286
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019960005683A KR100393913B1 (ko) | 1995-03-10 | 1996-03-05 | 5-메틸우리딘으로부터디4티를제조하는방법 |
Country Status (18)
Country | Link |
---|---|
US (1) | US5608049A (ko) |
EP (1) | EP0735044B1 (ko) |
JP (1) | JP3914279B2 (ko) |
KR (1) | KR100393913B1 (ko) |
CN (2) | CN1059213C (ko) |
AT (1) | ATE181556T1 (ko) |
AU (1) | AU694320B2 (ko) |
CA (1) | CA2170968A1 (ko) |
CY (1) | CY2155B1 (ko) |
DE (1) | DE69602983T2 (ko) |
DK (1) | DK0735044T3 (ko) |
ES (1) | ES2135168T3 (ko) |
GR (1) | GR3031243T3 (ko) |
HK (1) | HK1002979A1 (ko) |
HU (1) | HU220700B1 (ko) |
IL (1) | IL117225A (ko) |
SG (1) | SG38948A1 (ko) |
TW (1) | TW527359B (ko) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5608048A (en) * | 1995-06-05 | 1997-03-04 | Bristol-Myers Squibb Company | d4 T polymorphic Form 1 process |
WO2002020538A2 (en) * | 2000-09-06 | 2002-03-14 | Bristol-Myers Squibb Company | Stavudine polymorphic form 1 process |
AU2004275770A1 (en) * | 2003-09-22 | 2005-04-07 | Acidophil Llc | Small molecule compositions and methods for increasing drug efficiency using compositions thereof |
US7160537B2 (en) * | 2003-12-15 | 2007-01-09 | Siemens Medical Solutions Usa, Inc. | Method for preparing radiolabeled thymidine having low chromophoric byproducts |
US20050131224A1 (en) * | 2003-12-15 | 2005-06-16 | Cti Pet Systems, Inc. | Method for preparing radiolabeled thymidine |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3817982A (en) * | 1971-12-29 | 1974-06-18 | Syntex Inc | 2{40 ,3{40 -unsaturated nucleosides and method of making |
US4904770A (en) * | 1988-03-24 | 1990-02-27 | Bristol-Myers Company | Production of 2',3'-dideoxy-2',3'-didehydronucleosides |
JP3128080B2 (ja) * | 1991-10-02 | 2001-01-29 | 日本製紙株式会社 | 核酸化合物の新規な製造方法 |
US5539099A (en) * | 1993-11-15 | 1996-07-23 | Bristol-Myers Squibb Company | Process for large-scale preparation of 2',3'-didehydro-2',3'-dideoxynucleosides |
US5672698A (en) * | 1993-11-15 | 1997-09-30 | Bristol-Myers Squibb Co. | Preparation of 2',3'-didehydro-3'-deoxythymidine from 5-methyluridine |
-
1995
- 1995-03-10 US US08/402,283 patent/US5608049A/en not_active Expired - Lifetime
-
1996
- 1996-02-17 TW TW085102080A patent/TW527359B/zh not_active IP Right Cessation
- 1996-02-22 IL IL11722596A patent/IL117225A/en not_active IP Right Cessation
- 1996-03-04 CA CA002170968A patent/CA2170968A1/en not_active Abandoned
- 1996-03-05 JP JP04700596A patent/JP3914279B2/ja not_active Expired - Fee Related
- 1996-03-05 KR KR1019960005683A patent/KR100393913B1/ko not_active IP Right Cessation
- 1996-03-08 EP EP96301606A patent/EP0735044B1/en not_active Expired - Lifetime
- 1996-03-08 CN CN96105786A patent/CN1059213C/zh not_active Expired - Fee Related
- 1996-03-08 AU AU47982/96A patent/AU694320B2/en not_active Ceased
- 1996-03-08 DE DE69602983T patent/DE69602983T2/de not_active Expired - Fee Related
- 1996-03-08 ES ES96301606T patent/ES2135168T3/es not_active Expired - Lifetime
- 1996-03-08 DK DK96301606T patent/DK0735044T3/da active
- 1996-03-08 CN CNB001009850A patent/CN1195770C/zh not_active Expired - Fee Related
- 1996-03-08 HU HU9600607A patent/HU220700B1/hu not_active IP Right Cessation
- 1996-03-08 AT AT96301606T patent/ATE181556T1/de not_active IP Right Cessation
- 1996-03-09 SG SG1996006654A patent/SG38948A1/en unknown
-
1998
- 1998-03-05 HK HK98101842A patent/HK1002979A1/xx not_active IP Right Cessation
-
1999
- 1999-08-03 CY CY9900022A patent/CY2155B1/xx unknown
- 1999-09-16 GR GR990402335T patent/GR3031243T3/el unknown
Also Published As
Publication number | Publication date |
---|---|
CY2155B1 (en) | 2002-08-23 |
CN1059213C (zh) | 2000-12-06 |
CN1195770C (zh) | 2005-04-06 |
IL117225A0 (en) | 1996-06-18 |
HUP9600607A1 (en) | 1996-12-30 |
GR3031243T3 (en) | 1999-12-31 |
AU694320B2 (en) | 1998-07-16 |
AU4798296A (en) | 1996-09-19 |
EP0735044B1 (en) | 1999-06-23 |
HK1002979A1 (en) | 1998-09-30 |
CN1147519A (zh) | 1997-04-16 |
CA2170968A1 (en) | 1996-09-11 |
KR100393913B1 (ko) | 2003-12-18 |
DK0735044T3 (da) | 2000-01-10 |
ATE181556T1 (de) | 1999-07-15 |
SG38948A1 (en) | 1997-04-17 |
IL117225A (en) | 2001-04-30 |
DE69602983T2 (de) | 2000-03-09 |
EP0735044A1 (en) | 1996-10-02 |
DE69602983D1 (de) | 1999-07-29 |
CN1270172A (zh) | 2000-10-18 |
JP3914279B2 (ja) | 2007-05-16 |
JPH08269051A (ja) | 1996-10-15 |
HU220700B1 (hu) | 2002-04-29 |
TW527359B (en) | 2003-04-11 |
ES2135168T3 (es) | 1999-10-16 |
US5608049A (en) | 1997-03-04 |
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