Blog FDA approved small molecules

Synthesis of Difamilast (ADQUEY)

Patent / ApplicationTypeAssigneeFiledExpiry (~)
WO 2007/058338 A1 (US 7,919,617 B2; EP 1,953,148 B1; JP 4,975,757 B2)Composition of matter (originator)Otsuka Pharmaceutical Co., Ltd.2006-11-16 (priority 2005-11-15, JP 2005-330289)~Nov 2026 nominal (US 7,919,617 expiry ~2026-2027 absent PTE); PTE filing window opens at FDA approval (2026-02-12) — up to 5 yr PTE possible → effective LoE 2028–2031
WO 2010/041680 A1 / JP 5,628,114 B2Crystal form / polymorph (originator)Otsuka Pharmaceutical Co., Ltd.2009-10-07 (priority JP 2008-263071)~Oct 2029 nominal
WO 2017/170219 / JP 6,832,946 B2Topical formulationOtsuka Pharmaceutical Co., Ltd.~2017~2037 nominal
Process patent(s) — OtsukaProcessOtsuka Pharmaceutical Co., Ltd.~2008–2015~2028–2035
[Acrotech / Medimetriks licensing-related filings]License / territoryAcrotech Biopharma Inc (US); Medimetriks Pharmaceuticals (prior US rights holder for atopic dermatitis)

Compiled: 2026-05-23 · Trigger event: FDA approval, 2026-02-12 Innovator: Acrotech Biopharma Inc (US licensee; originator Otsuka Pharmaceutical Co., Ltd., Japan — OPA-15406 / MM-36) Status: Approved NME

Mechanism: Topical PDE4 (cAMP-specific phosphodiesterase 4) inhibitor with preferential PDE4B binding (ChEMBL CHEMBL2093863); inhibits cAMP hydrolysis in keratinocytes and T-cells → reduces pro-inflammatory cytokine release (TNF-α, IL-4, IL-5, IL-13). PMID 27189825 + 30386231

Synthesis Route of the Originator

Convergent synthesis disclosed in Otsuka WO 2007/058338 (Example 5). Eastern fragment is a 4-(difluoromethoxy)-3-isopropoxybenzamide (INT-2) that condenses with 1,3-dichloroacetone under Robinson-Gabriel conditions to give the 2-aryl-4-(chloromethyl)-1,3-oxazole (INT-3); azide displacement then Staudinger reduction (or hydrogenolysis) installs the 4-(aminomethyl) handle (INT-5). Final amide coupling of INT-5 with 2-ethoxybenzoyl chloride (or 2-ethoxybenzoic acid + HATU/EDC) delivers difamilast. Aryl SM (3,4-disubstituted benzonitrile/benzamide) is built from vanillin-class catechol via selective O-isopropylation then O-difluoromethylation of the residual phenol (ClCF₂H, base) — both transformations are commodity-scale.

Key intermediates

Crystal Forms, Salts, and Solid-State Profile

  • API in approved drug product: free base (anhydrous, white-to-off-white crystalline solid; per ADQUEY label)
  • Strengths approved: 1% ointment (10 mg difamilast / g; topical, BID dosing)
  • Third-party polymorph activity: No US-filed third-party polymorph activity identified as of 2026-05-23 — atypical given imminent NCE clock; monitor SureChEMBL and Espacenet quarterly
  • Originator polymorph filing: WO 2010/041680 / JP 5,628,114 (Otsuka) — claims specific anhydrous Form I and a hydrate; Orange Book listing pending FDA approval-stage publication

Key peer-reviewed literature