Lta4h inhibitors for the treatment of hidradenitis suppurativa
A technology of hidradenitis suppurativa and inhibitors, applied in the direction of medical preparations containing active ingredients, pill delivery, organic active ingredients, etc., which can solve problems such as debility
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Embodiment 2
[0099]Embodiment 2A relates to the method of embodiment 2 comprising administering to the subject a therapeutically effective amount of a compound of formula (II) or a pharmaceutically acceptable salt thereof,
[0100]
[0101] wherein the variables R1, R2 and Y have the meanings as defined in Example 1.
[0102] Embodiment 2B relates to the method of embodiment 2 comprising administering to the subject a therapeutically effective amount of a compound of formula (III) or a pharmaceutically acceptable salt thereof,
[0103]
[0104] wherein the variables R1, R2 and Y have the meanings as defined in Example 1.
[0105] Embodiment 2C is directed to the method of embodiment 2, comprising administering to the subject a therapeutically effective amount of a compound of formula (IV) or a pharmaceutically acceptable salt thereof,
[0106]
[0107] wherein the variables R1, R2 and Y have the meanings as defined in Example 1.
[0108] Embodiment 2D is directed to the method o...
example 1
[0368] Example 1: (S)-3-amino-4-(5-(4-((5-chloro-3-fluoropyridin-2-yl)oxy)phenyl)-2H-tetrazol-2-yl) Butyric Acid (Form B)
[0369]
[0370] Example 29 (28 g, 35 mmol) as described in WO 2015 / 092740 and a solvent mixture containing 360 g water and 40 g THF were mixed together and stirred for 20 minutes. The mixture was filtered and washed with aqueous NaHCO 3 The filtrate was adjusted to pH=5. Stirring was continued for 18 h before the mixture was filtered to give 25.6 g of the free acid (Int-1 ) in a wet cake which was used without further purification to prepare polymorph Form B. 505 mg of free acid (Int-1) was weighed into a 20 ml glass vial and 6 mL of methanol was added. The slurry was heated to 50 °C and stirred using a magnetic stirrer for 4 days. The suspension was cooled to room temperature and filtered. The recovered solid was dried under vacuum at 40 °C for 2.5 h. The white solid was analyzed by XRPD, DSC and TGA (respectively Figure 1-3 ).
[0371] An al...
example 2
[0386] Compound of Example 1 as a formulation of capsules
[0387]
[0388] 1 of vegetable origin
[0389] 2 removed during processing
[0390] 3 The composition of the capsule shell is given in the table below
[0391] Components of a capsule shell
[0392]
[0393] E: Refers to the official number used by the European Union for colorants
[0394] Regulation (EU) 231 / 2012: Commission Regulation (EU) laying down the specifications for food additives. Capsules were purchased from Lonza (now Capsugel)
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