참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Zidovudine guanidine | HCID 15817654 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | Zidovudine | HCID 35370 | — |
반응 단계
The zidovudine guanidine salts from each of Compositions E and F were combined and thereafter added to a mixture of water (23 mL) and 32% hydrochloric acid (7.98 g) which had been heated to 85° C. The salts were completely dissolved in a few minutes and the pH of the mixture was 8.2. The pH was then adjusted to pH 1 by further addition of 32% hydrochloric acid the mixture was then cooled to ambient temperature and stirred for 16 hours. Thereafter, the mixture was further cooled to 5° C., stirred for 30 minutes, and filtered and washed with water to yield 15.74 g of substantially purified zidovudine--see Composition H in Table 1. The mother liquor from the production of Composition H was basified to pH 12.35 by addition of 50% sodium hydroxide to yield a precipitate which was filtered and washed with water to yield 2.18 g of zidovudine guanidine salt--see Composition I in Table 1--which was of sufficient purity to be recycled with other batches of zidovudine guanidine salts (i.e. combine with salts from Compositions E and F). The mother liquor was acidified to pH 1 and extracted several times with methyl isobutyl ketone and the combined extract was set aside.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05519129 |
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| 출처 데이터셋 | uspto-grants-1996_05 |
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| ORD ID | ord-6c99c719de2d4ab982c211c84305ffbd |
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| 출처 메모 | uspto-grants-1996_05 |
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