関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Erlotinib | HCID 176870 | — |
| 溶媒 | 1-Pentanol | HCID 6276 | — |
| 生成物 | Erlotinib Hydrochloride | HCID 176871 | 90% |
反応手順
115 g (0.292 mol) of erlotinib base was added to 2300 ml (20 vol) of 1-pentanol at 25-30° C. The mixture was cooled to 5 to 10° C. and stirred for 30 min. to obtain a suspension. 57.5 g of aqueous hydrochloric acid at a concentration of 35% (w/w) was added drop wise at 5-10° C. and the mixture stirred for 1 hour. The product was isolated by filtration and washed with 230 ml (2 vol.) of 1-pentanol. The product was dried under reduced pressure (50 mm Hg) at 0-60° C. to obtain 113 g of erlotinib hydrochloride polymorph A as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09340515B2 |
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| 出典データセット | uspto-grants-2016_05 |
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| ORD ID | ord-d2aa1b856f7a4a12be5b88ef642f98af |
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| 出典メモ | uspto-grants-2016_05 |
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