JP2023513731A - キラルベンゾジアゼピノン誘導体の調製方法 - Google Patents

キラルベンゾジアゼピノン誘導体の調製方法 Download PDF

Info

Publication number
JP2023513731A
JP2023513731A JP2022548818A JP2022548818A JP2023513731A JP 2023513731 A JP2023513731 A JP 2023513731A JP 2022548818 A JP2022548818 A JP 2022548818A JP 2022548818 A JP2022548818 A JP 2022548818A JP 2023513731 A JP2023513731 A JP 2023513731A
Authority
JP
Japan
Prior art keywords
compound
formula
solvent
represented
combination
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.)
Pending
Application number
JP2022548818A
Other languages
English (en)
Japanese (ja)
Other versions
JP2023513731A5 (https=
Inventor
チマルスティ、クリストファー・エム
ラホティ、アーナンドクマール・マダンラル
ラジャ ゴーパール レッディ ダラム、マダン
Original Assignee
アヤラ ファーマシューティカルズ インコーポレイテッド
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 アヤラ ファーマシューティカルズ インコーポレイテッド filed Critical アヤラ ファーマシューティカルズ インコーポレイテッド
Publication of JP2023513731A publication Critical patent/JP2023513731A/ja
Publication of JP2023513731A5 publication Critical patent/JP2023513731A5/ja
Pending legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/24Oxygen or sulfur atoms
    • C07D207/262-Pyrrolidones
    • C07D207/2732-Pyrrolidones with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to other ring carbon atoms
    • C07D207/277Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D207/282-Pyrrolidone-5- carboxylic acids; Functional derivatives thereof, e.g. esters, nitriles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D243/00Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
    • C07D243/06Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
    • C07D243/10Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
    • C07D243/141,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines
    • C07D243/161,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals
    • C07D243/181,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals substituted in position 2 by nitrogen, oxygen or sulfur atoms
    • C07D243/24Oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D243/00Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
    • C07D243/06Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
    • C07D243/10Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
    • C07D243/141,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines
    • C07D243/161,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals
    • C07D243/181,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals substituted in position 2 by nitrogen, oxygen or sulfur atoms
    • C07D243/24Oxygen atoms
    • C07D243/26Preparation from compounds already containing the benzodiazepine skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D243/00Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
    • C07D243/06Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
    • C07D243/10Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
    • C07D243/141,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines
    • C07D243/161,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals
    • C07D243/181,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals substituted in position 2 by nitrogen, oxygen or sulfur atoms
    • C07D243/24Oxygen atoms
    • C07D243/30Preparation including building-up the benzodiazepine skeleton from compounds already containing hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
JP2022548818A 2020-02-16 2021-02-16 キラルベンゾジアゼピノン誘導体の調製方法 Pending JP2023513731A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US202062977316P 2020-02-16 2020-02-16
US62/977,316 2020-02-16
PCT/US2021/018137 WO2021163676A1 (en) 2020-02-16 2021-02-16 Methods of preparing chiral benzodiazepinone derivatives

Publications (2)

Publication Number Publication Date
JP2023513731A true JP2023513731A (ja) 2023-04-03
JP2023513731A5 JP2023513731A5 (https=) 2024-02-22

Family

ID=77291712

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2022548818A Pending JP2023513731A (ja) 2020-02-16 2021-02-16 キラルベンゾジアゼピノン誘導体の調製方法

Country Status (11)

Country Link
US (2) US12503449B2 (https=)
EP (1) EP4107148A4 (https=)
JP (1) JP2023513731A (https=)
KR (1) KR20220143094A (https=)
CN (1) CN115103836A (https=)
AU (1) AU2021218456A1 (https=)
BR (1) BR112022016249A2 (https=)
CA (1) CA3171651A1 (https=)
IL (1) IL295572A (https=)
MX (1) MX2022010079A (https=)
WO (1) WO2021163676A1 (https=)

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6323824A (ja) * 1986-07-14 1988-02-01 メルク エンド カムパニ− インコ−ポレ−テツド 酸性α−水素を有するアミンの光学分割およびラセミ化方法
JPH05178805A (ja) * 1990-02-16 1993-07-20 Dsm Nv 光学的に活性なアミノ酸アミドの製法
JP2009508830A (ja) * 2005-09-19 2009-03-05 アロー セラピューティクス リミテッド C型肝炎感染症を治療するためのベンゾジアゼピン誘導体
WO2010073253A1 (en) * 2008-12-22 2010-07-01 Natco Pharma Limited Method for preparing an optically active frovatriptan
JP2015529253A (ja) * 2012-09-21 2015-10-05 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company Notch阻害剤としてのフルオロアルキルおよびフルオロシクロアルキル1,4−ベンゾジアゼピノン化合物
JP2015529252A (ja) * 2012-09-21 2015-10-05 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company フルオロアルキル−1,4−ベンゾジアゼピノン化合物
JP2015530411A (ja) * 2012-09-21 2015-10-15 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company Notch阻害剤としてのビス(フルオロアルキル)−1,4−ベンゾジアゼピノン化合物
JP2015534554A (ja) * 2012-09-21 2015-12-03 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company アルキル,フルオロアルキル−1,4−ベンゾジアゼピノン化合物
CN105439939A (zh) * 2015-11-12 2016-03-30 四川恒康科技发展有限公司 一种(S)-N-Boc-3-羟基哌啶的合成方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0751555B2 (ja) 1992-04-15 1995-06-05 キヤノン株式会社 ジイモニウム塩化合物
WO2013148554A1 (en) * 2012-03-30 2013-10-03 Merck Sharp & Dohme Corp. Process for preparing fluoroleucine alkyl esters
JP6687596B2 (ja) 2015-02-17 2020-04-22 アモーレパシフィック コーポレーションAmorepacific Corporation N−[4−(1−アミノエチル)−フェニル]−スルホンアミド誘導体のキラル分割方法

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6323824A (ja) * 1986-07-14 1988-02-01 メルク エンド カムパニ− インコ−ポレ−テツド 酸性α−水素を有するアミンの光学分割およびラセミ化方法
JPH05178805A (ja) * 1990-02-16 1993-07-20 Dsm Nv 光学的に活性なアミノ酸アミドの製法
JP2009508830A (ja) * 2005-09-19 2009-03-05 アロー セラピューティクス リミテッド C型肝炎感染症を治療するためのベンゾジアゼピン誘導体
WO2010073253A1 (en) * 2008-12-22 2010-07-01 Natco Pharma Limited Method for preparing an optically active frovatriptan
JP2015529253A (ja) * 2012-09-21 2015-10-05 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company Notch阻害剤としてのフルオロアルキルおよびフルオロシクロアルキル1,4−ベンゾジアゼピノン化合物
JP2015529252A (ja) * 2012-09-21 2015-10-05 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company フルオロアルキル−1,4−ベンゾジアゼピノン化合物
JP2015530411A (ja) * 2012-09-21 2015-10-15 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company Notch阻害剤としてのビス(フルオロアルキル)−1,4−ベンゾジアゼピノン化合物
JP2015534554A (ja) * 2012-09-21 2015-12-03 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company アルキル,フルオロアルキル−1,4−ベンゾジアゼピノン化合物
CN105439939A (zh) * 2015-11-12 2016-03-30 四川恒康科技发展有限公司 一种(S)-N-Boc-3-羟基哌啶的合成方法

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
化学便覧 応用化学編 第5版, vol. 第2刷, JPN6024043327, 2001, pages 320 - 322, ISSN: 0005577390 *

Also Published As

Publication number Publication date
CN115103836A (zh) 2022-09-23
MX2022010079A (es) 2022-09-02
US20250346565A1 (en) 2025-11-13
BR112022016249A2 (pt) 2022-10-11
CA3171651A1 (en) 2021-08-19
EP4107148A1 (en) 2022-12-28
WO2021163676A1 (en) 2021-08-19
EP4107148A4 (en) 2024-05-15
IL295572A (en) 2022-10-01
US20230108536A1 (en) 2023-04-06
US12503449B2 (en) 2025-12-23
AU2021218456A1 (en) 2022-09-22
KR20220143094A (ko) 2022-10-24

Similar Documents

Publication Publication Date Title
KR100937915B1 (ko) 변형된 픽텟-스펭글러 반응 및 그것으로부터 제조된생성물
JP2010540614A (ja) モナチン鏡像異性体の生成
EP2595976A1 (fr) Procede de preparation de derives d'amino-benzoyl-benzofurane
EP2142501B1 (fr) Procede de preparation de derives de porphyrine, telle que la protoporphyrine (ix) et intermediaire de synthese
WO2017191539A1 (en) Process for the preparation dl-proline co-crystal of dapagliflozin
CN101563329A (zh) 用于制备4,4’-(1-甲基-1,2-乙二基)-双-(2,6-哌嗪二酮)的新方法
JP2023513731A (ja) キラルベンゾジアゼピノン誘導体の調製方法
CA2261829C (fr) Intermediaires pour la preparation de 2-imidazoline-5-ones
Golliher et al. The synthesis and use of γ-chloro-enamides for the subsequent construction of novel enamide-containing small molecules
JP2008505175A (ja) ピロロトリアジン化合物の製造法
JPH11512412A (ja) 光学活性α−アミノ酸およびα−アミノ酸誘導体の製造方法
WO2022232060A1 (en) Processes for the synthesis of valbenazine
CA2668026A1 (fr) Derives d' aminobenzocycloheptene, leurs procedes de preparation et leur utilisation en therapeutique
CN1984881B (zh) 制备对映体形式2,3-二氨基丙酸衍生物的方法
EP2938595B1 (fr) Procede de synthese d'une hydrazine utile dans le traitement du virus du papillome
WO2001066530A1 (fr) URETHANE N-CARBOXYANHYDRIDES ISSUS DE β-AMINOACIDES, LEUR PROCEDE DE PREPARATION ET LEURS UTILISATIONS.
JP2005255610A (ja) 光学活性な3−アミノアスパラギン酸誘導体の製造方法
HK1101820A (en) Method for producing enantiomeric form of 2,3-diaminopropionic acid derivatives
EP2300405A1 (fr) Procédés de synthèse asymétrique de la 6-fluoro-l-dopa et de ses analogues
WO2006093354A1 (ja) (s)−2−[3−(n−{[4−(4−フルオロフェノキシ)フェニル]メチル}カルバモイル)−4−メトキシフェニルメチル]ブタン酸の製造中間体

Legal Events

Date Code Title Description
A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20240214

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20240214

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20250422

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20250718

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20250918

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20251017

A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20251209

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20260406