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HRID 631038作成日:2026年10月26日

Mannitol → Bendamustine Mannitol

https://huagongshe.com/reaction/631038

反応式

関与物質

役割名称HCID仕込み量
反応物MannitolHCID 6251—
反応物BendamustineHCID 65628—
反応物Bendamustine HydrochlorideHCID 77082—
反応物Ethanol bendamustineHCID 131735415—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒1-PropanolHCID 1031—
生成物Bendamustine MannitolHCID 131735414—

反応手順

Two batches (Batch 1 and Batch2) each one with a different pharmaceutical composition comprising solid dispersions in the form of dry powder and substantially free of hydrolysis degradants were produced. For each batch, two pre-drying intermediate compositions were formulated in separate containers. For Batch 1, the aqueous pre-drying composition was formulated consisting of 2380 mg of mannitol dissolved in 70 ml of water. The non-aqueous pre-drying composition was formulated by dissolving 1400 mg of bendamustine in 70 ml of n-propanol. For Batch 2, the aqueous pre-drying composition consisted of 1190 mg of mannitol dissolved in 70 ml of water. The non-aqueous pre-drying composition was formulated by dissolving 700 mg of bendamustine hydrochloride in 70 ml of ethanol. The ethanol/bendamustine solution could be cooled to minimize the extent of possible side reactions. Both feed pumps (see FIG. 10) were set in such a way that the ratio of excipient to API was 1.8 for Batch 1 and 1.9 for Batch 2. Tables 2 and 3 show the process parameters for Batch 1 and Batch 2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09320730B2
出典データセットuspto-grants-2016_04
ORD IDord-1ca2d6f0ffff47bfafbea48a9b07efc3
出典メモuspto-grants-2016_04