CH4630808
syn https://newdrugapprovals.org/2018/07/02/ch4630808/
Paper
Development of a Kilogram-Scale Synthesis of a Novel Anti-HCV Agent, CH4930808
CH4630808 corrected
† Research Division, Chugai Pharmaceutical Co., Ltd., 1-135 Komakado, Gotemba, Shizuoka 412-8513, Japan
‡ Pharmaceutical Technology Division, Chugai Pharmaceutical Co., Ltd., 5-5-1 Ukima, Kita-ku, Tokyo 115-8543, Japan
§ Department of Chemistry for Materials, Graduate School of Engineering, Mie University, Tsu, Mie 514-8507, Japan
Org. Process Res. Dev., 2018, 22 (2), pp 236–240
DOI: 10.1021/acs.oprd.7b00383
Abstract
![Abstract Image](https://pubs.acs.org/appl/literatum/publisher/achs/journals/content/oprdfk/2018/oprdfk.2018.22.issue-2/acs.oprd.7b00383/20180212/images/medium/op-2017-00383d_0007.gif)
Herein, we report the kilogram-scale synthesis of CH4930808 (1) CH 4630808 CORRECTED, a novel anti-hepatitis C virus agent. While pursuing improved productivity using many through-process strategies, we conducted scrupulous impurity control. Finally, we successfully developed a practical and scalable process for the synthesis of (1·1.5Na·2.5H2O), by which we prepared 3.28 kg of the active pharmaceutical ingredient for clinical studies
1H-NMR and 13C-NMR spectra of compound 5·HCl S 3– S 4
![](https://i1.wp.com/drugapprovalsint.com/wp-content/uploads/2018/07/str1.jpg)
![](https://i0.wp.com/drugapprovalsint.com/wp-content/uploads/2018/07/str2.jpg)
1H-NMR spectra of compound 1·1.5 Na·2.5 H2O S 5
![](https://i0.wp.com/drugapprovalsint.com/wp-content/uploads/2018/07/str1-1.jpg)
![](https://i2.wp.com/drugapprovalsint.com/wp-content/uploads/2018/07/str1-10.jpg)
![](https://i1.wp.com/drugapprovalsint.com/wp-content/uploads/2018/07/str2-4.jpg)
13C-NMR spectra compound 1·1.5 Na·2.5 H2O S 6
![](https://i0.wp.com/drugapprovalsint.com/wp-content/uploads/2018/07/str1-2.jpg)
![](https://i2.wp.com/drugapprovalsint.com/wp-content/uploads/2018/07/str1-11.jpg)
![](https://i1.wp.com/drugapprovalsint.com/wp-content/uploads/2018/07/str2-5.jpg)
1H-COSY spectra of compound 1·1.5 Na·2.5 H2O S 7 – S 8
![](https://i1.wp.com/drugapprovalsint.com/wp-content/uploads/2018/07/str1-4.jpg)
![](https://i0.wp.com/drugapprovalsint.com/wp-content/uploads/2018/07/str1-3.jpg)
DEPT spectra of compound 1·1.5 Na·2.5 H2O S 9 – S 10
![](https://i1.wp.com/drugapprovalsint.com/wp-content/uploads/2018/07/str1-5.jpg)
![](https://i2.wp.com/drugapprovalsint.com/wp-content/uploads/2018/07/str1-6.jpg)
HMBC spectra of compound 1·1.5 Na·2.5 H2O S 11 – S 17
![](https://i0.wp.com/drugapprovalsint.com/wp-content/uploads/2018/07/str3.jpg)
![](https://i0.wp.com/drugapprovalsint.com/wp-content/uploads/2018/07/str1-8.jpg)
![](https://i1.wp.com/drugapprovalsint.com/wp-content/uploads/2018/07/str2-2.jpg)
![](https://i2.wp.com/drugapprovalsint.com/wp-content/uploads/2018/07/str1-9.jpg)
![](https://i1.wp.com/drugapprovalsint.com/wp-content/uploads/2018/07/str2-3.jpg)
MASS
![](https://i1.wp.com/drugapprovalsint.com/wp-content/uploads/2018/07/str1-12.jpg)
////////////////
No comments:
Post a Comment