참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Oxalic acid dihydrate | HCID 61373 | — |
| 반응물 | Escitalopram | HCID 146570 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 생성물 | Escitalopram Oxalate | HCID 146571 | — |
반응 단계
100 g of the free base was dissolved in 250 mL of 2-propanol. 1 eq. of oxalic acid dihydrate was dissolved in 250 mL of warm 2-propanol and was added at 40° C. to the solution of escitalopram base. After stirring at 40° C. for 10 min the crystallization started. The mixture was then allowed to cool to room temperature and stirred for ca. 2 hours. The crystals were filtered off, rinsed on the filter with 2-propanol and dried to constant weight under vacuum at 60° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07834201B2 |
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| 출처 데이터셋 | uspto-grants-2010_11 |
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| ORD ID | ord-2f5dc779cec14e3fb4083b9544b5a79c |
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| 출처 메모 | uspto-grants-2010_11 |
|---|