CN107522701B — 一种治疗慢性淋巴细胞白血病的BTK抑制剂Acalabrutinib的合成方法
Assigned to SUZHOU FUSHILAI PHARMACEUTICAL Co Ltd · Expires 2019-11-08 · 7y expired
What this patent protects
一种治疗慢性淋巴细胞白血病的BTK抑制剂Acalabrutinib的合成方法,步骤:制备(S)‑2‑(8‑氨基咪唑并[1,5‑a]吡嗪‑3‑基)‑1‑吡咯烷甲酸苄酯;制备(S)‑2‑(8‑叔丁氧羰基氨基咪唑并[1,5‑a]吡嗪‑3‑基)‑1‑吡咯烷甲酸苄酯;制备(S)‑2‑(8‑叔丁氧羰基氨基‑1‑溴咪唑并[1,5‑a]吡嗪‑3‑基)‑1‑吡咯烷甲酸苄酯;制备(S)‑2‑{8‑叔丁氧羰基氨基‑1‑[4‑(2‑吡啶基氨甲酰基)苯基]咪唑并[1,5‑a]吡嗪‑3‑基}‑1‑吡咯烷甲酸苄酯;制备(S)‑2‑{8‑叔丁氧羰基氨基‑1‑[4‑(2‑吡啶基氨甲酰基)…
USPTO Abstract
一种治疗慢性淋巴细胞白血病的BTK抑制剂Acalabrutinib的合成方法,步骤:制备(S)‑2‑(8‑氨基咪唑并[1,5‑a]吡嗪‑3‑基)‑1‑吡咯烷甲酸苄酯;制备(S)‑2‑(8‑叔丁氧羰基氨基咪唑并[1,5‑a]吡嗪‑3‑基)‑1‑吡咯烷甲酸苄酯;制备(S)‑2‑(8‑叔丁氧羰基氨基‑1‑溴咪唑并[1,5‑a]吡嗪‑3‑基)‑1‑吡咯烷甲酸苄酯;制备(S)‑2‑{8‑叔丁氧羰基氨基‑1‑[4‑(2‑吡啶基氨甲酰基)苯基]咪唑并[1,5‑a]吡嗪‑3‑基}‑1‑吡咯烷甲酸苄酯;制备(S)‑2‑{8‑叔丁氧羰基氨基‑1‑[4‑(2‑吡啶基氨甲酰基)苯基]咪唑并[1,5‑a]吡嗪‑3‑基}吡咯烷;制备(S)‑2‑{8‑叔丁氧羰基氨基‑1‑[4‑(2‑吡啶基氨甲酰基)苯基]咪唑并[1,5‑a]吡嗪‑3‑基}‑1‑(2‑丁炔酰基)吡咯烷;制备Acalabrutinib。收率高;简化流程;绿色环保。
Drugs covered by this patent
- Calquence (ACALABRUTINIB) · AstraZeneca
Bibliographic data sourced from FDA Orange Book + USPTO public records. Plain-English summary generated by AI grounded in source text. Patent term extensions (PTR, SPC, pediatric) may shift the effective expiry. Not legal advice.
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