HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863089Generated: October 26, 2026
Nordiazepam → 7-chloro-1,3-dihydro-1-[3-(2-methyl-1,3-dioxolan-2-yl)propyl]-5-phenyl-2H-1,4-benzodiazepin-2-one
https://huagongshe.com/reaction/1863089
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nordiazepam | HCID 2997 | — |
| Reactant | 2-(3-Chloropropyl)-2-methyl-1,3-dioxolane | HCID 80079 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-chloro-1,3-dihydro-1-[3-(2-methyl-1,3-dioxolan-2-yl)propyl]-5-phenyl-2H-1,4-benzodiazepin-2-one | HCID 20393360 | — |
Reaction Steps
A solution of 54.2 g. of 7-chloro-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepin-2-one in 500 ml. of dimethylformamide is treated under an atmosphere of argon at 0° C. with 32.8 g. of potassium tertiary butylate and the mixture is then stirred in an ice-bath for 30 minutes. Then, at 10°-15° C. there is added a solution of 66 g. of 2-(3-chloropropyl)-2-methyl-1,3-dioxolan in 100 ml. of dimethylformamide, the mixture is stirred at 20°-25° C. for 30 minutes and subsequently heated to 100° C. for 30 minutes. The mixture is cooled and poured on to 2.5 liters of ice-water. The separated oily product is extracted with methylene chloride and the organic phase washed with a saturated aqueous sodium chloride solution, dried over sodium sulfate and concentrated to dryness. The residue crystallizes upon trituration with ether, and there is obtained 7-chloro-1,3-dihydro-1-[3-(2-methyl-1,3 -dioxolan-2-yl)propyl]-5-phenyl-2H-1,4-benzodiazepin-2-one having a melting point of 152°-153° C. Recrystallization from ethanol does not increase the melting point.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04167632 |
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| Source dataset | uspto-grants-1979_09 |
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| ORD ID | ord-44d157d88420434f976a10d22bd2f93c |
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| Source note | uspto-grants-1979_09 |
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