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HRID 1658608作成日:2026年10月25日
Clonazepam → 11b-(2-chlorophenyl)-10-nitro-2,3,5,11b-tetrahydrooxazolo[3,2-d][1,4]benzodiazepin-6(7H)-one
https://huagongshe.com/reaction/1658608
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Clonazepam | HCID 2802 | — |
| 反応物 | Ethylene Oxide | HCID 6354 | — |
| 反応物 | Ammonium Hydroxide | HCID 14923 | — |
| 溶媒 | 1,2-Dichloroethane | HCID 11 | — |
| 生成物 | 11b-(2-chlorophenyl)-10-nitro-2,3,5,11b-tetrahydrooxazolo[3,2-d][1,4]benzodiazepin-6(7H)-one | HCID 12317902 | — |
反応手順
A solution of 5.2 g of (0.02 M) of stannic chloride in 60 ml of dry ethylene dichloride under nitrogen was treated with 2.9 g (0.0091 M) of 5-(2-chlorophenyl)-1,3-dihydro-7-nitro-2H-1,4-benzodiazepin-2-one. The reaction was cooled in an ice bath, and 2.6 g (0.06 M) of ethylene oxide in 10 ml of ethylene dichloride was added with stirring over an 8 min period. After 18 hr at room temperature, the solution was made basic with concentrated ammonium hydroxide and filtered. The filtrates were washed with a saturated solution of brine, dried over anhydrous sodium sulfate and evaporated to dryness. The residue was crystallized from a mixture of dichloromethane, methanol and petroleum ether to give the above named product as white rods, melting at 201°-203°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US03965151 |
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| 出典データセット | uspto-grants-1976_06 |
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| ORD ID | ord-04f15e6fd4774174ad1ae4a2134a164d |
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| 出典メモ | uspto-grants-1976_06 |
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