トホグリフロジン水和物

トホグリフロジン水和物 化学構造式
1201913-82-7
CAS番号.
1201913-82-7
化学名:
トホグリフロジン水和物
别名:
トホグリフロジン水和物;トホグリフロジン水和物 (JAN)
英語名:
TOFOGLIFLOZIN
英語别名:
Tofogliflozin Monohydrate;CSG452; CSG-452; TOFOGLIFLOZIN; CSG 452; UNII-554245W62TTOFOGLIFLOZIN [INN]; TOFOGLIFLOZIN ANYHYDROUS;Togliflozin;CSG 452(hydrate);Tofogliflozin(CSG452);Tofogliflozin (hydrate);TOFOGLIFLOZIN USP/EP/BP;Tofogliflozin anyhydrous;Tofogliflozin Hydrate (JAN);Tofogliflozin hydrate (1:1)
CBNumber:
CB92667680
化学式:
C22H26O6.H2O
分子量:
404.46
MOL File:
1201913-82-7.mol

トホグリフロジン水和物 物理性質

貯蔵温度 :
Store at -20°C
溶解性:
DMF: 30 mg/ml; DMSO: 30 mg/ml; Ethanol: 30 mg/ml; Ethanol:PBS (pH7.2)(1:20): 0.05 mg/ml
外見 :
A crystalline solid
安全性情報
  • リスクと安全性に関する声明
  • 危険有害性情報のコード(GHS)
絵表示(GHS) GHS hazard pictograms
注意喚起語 警告
危険有害性情報
コード 危険有害性情報 危険有害性クラス 区分 注意喚起語 シンボル P コード
H302 飲み込むと有害 急性毒性、経口 4 警告 GHS hazard pictograms P264, P270, P301+P312, P330, P501
H315 皮膚刺激 皮膚腐食性/刺激性 2 警告 GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 強い眼刺激 眼に対する重篤な損傷性/眼刺激 性 2A 警告 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 呼吸器への刺激のおそれ 特定標的臓器毒性、単回暴露; 気道刺激性 3 警告 GHS hazard pictograms
注意書き
P261 粉じん/煙/ガス/ミスト/蒸気/スプレーの吸入を避ける こと。
P305+P351+P338 眼に入った場合:水で数分間注意深く洗うこと。次にコ ンタクトレンズを着用していて容易に外せる場合は外す こと。その後も洗浄を続けること。

トホグリフロジン水和物 価格

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入

トホグリフロジン水和物 化学特性,用途語,生産方法

効能

糖尿病治療薬, SGLT-2阻害薬

商品名

アプルウェイ (サノフィ); デベルザ (興和)

説明

Tofogliflozin hydrate, which is a sodium-glucose co-transporter 2 inhibitor, was approved in Japan for the treatment of type 2 diabetes at the same time as luseogliflozin hydrate (XIX). The drug was discovered by Chugai Pharmaceutical and jointly developed with Sanofi-Aventis and Kowa. Tofogliflozin hydrate reduces glucose levels by inhibiting the reuptake of glucose by selectively inhibiting SGLT2, and plays a key role in the reuptake of glucose in the proximal tubule of the kidneys.

合成

Reduction of commercially available 2-bromoterephtalic acid (268) through the use of trimethoxyborane and borane- THF proceeded in 89% yield to afford diol 269. Subjection of this compound to 2-methoxypropene (270) under acidic conditions generated bis-acetonide 271. This bromide then underwent lithium¨Chalogen exchange followed by exposure to magnesium bromide and treatment with lactone 272 (which was prepared by persilylation of commercially available (3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2Hpyran- 2-one (277). This mixture was worked up with aqueous ammonium chloride and upon treatment with p-TsOH in methanol resulted in spiroacetal 273. Next, global protection of all alcohol functionalities within 273 was affected by reaction with methylchloroformate and DMAP in acetonitrile. The benzyl carbonate within 274 was selectively exchanged via Suzuki coupling with 4-ethylphenylboronic acid (275) to afford methylene dibenzyl system 276. Subsequent treatment with aqueous sodium hydroxide in methanol followed by crystallization from 1:6 acetone and water furnished the desired product tofogliflozin hydrate (XXXIV) in 75% yield.

説明図

トホグリフロジン水和物 上流と下流の製品情報

原材料

準備製品


トホグリフロジン水和物 生産企業

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トホグリフロジン水和物  スペクトルデータ(1HNMR)


1201913-82-7(トホグリフロジン水和物)キーワード:


  • 1201913-82-7
  • Tofogliflozin (hydrate)
  • (1S,3'R,4'S,5'S,6'R)-6-[(4-Ethylphenyl)methyl]-3',4',5',6'-tetrahydro-6'-(hydroxymethyl)spiro[isobenzofuran-1(3H),2'-[2H]pyran]-3',4',5'-triol hydrate (1:1)
  • Tofogliflozin hydrate (1:1)
  • Tofogliflozin hydrate (1:1)-API
  • Tofogliflozin anyhydrous
  • UNII-554245W62TTofogliflozin [INN]
  • CSG 452(hydrate)
  • (3S,3'R,4'S,5'S,6'R)-5-[(4-ethylphenyl)methyl]-6'-(hydroxymethyl)spiro[1H-2-benzofuran-3,2'-oxane]-3',4',5'-triol,hydrate
  • Tofogliflozin(CSG452)
  • Tofogliflozin Hydrate (JAN)
  • Tofogliflozin hydrate (CSG-452 hydrate)
  • TOFOGLIFLOZIN USP/EP/BP
  • Tofogliflozin Monohydrate
  • CSG452; CSG-452; TOFOGLIFLOZIN; CSG 452; UNII-554245W62TTOFOGLIFLOZIN [INN]; TOFOGLIFLOZIN ANYHYDROUS
  • Togliflozin
  • Tofogliflozin Monohydrate(CSG 452 hydrate)
  • トホグリフロジン水和物
  • トホグリフロジン水和物 (JAN)
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