HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465072Generated: October 29, 2026
Carbonate Ion → 11-[[3-[(Diethylamino)methyl]-1-piperidinyl]acetyl]-5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one
https://huagongshe.com/reaction/465072
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbonate Ion | HCID 19660 | — |
| Reactant | 11-(Chloroacetyl)-5,11-dihydro-6H-pyrido(2,3-b)(1,4)benzodiazepin-6-one | HCID 120053 | — |
| Reactant | Diethyl-piperidin-3-ylmethyl-amine | HCID 6484181 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 11-[[3-[(Diethylamino)methyl]-1-piperidinyl]acetyl]-5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one | HCID 13578571 | — |
Reaction Steps
A solution of 3-[(diethylamino)-methyl]piperidine (4.6 g, 0.027 mol) in dry dimethylformamide (10 ml) is added dropwise over 2 hours to a suspension of 11-chloroacetyl-5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one (5.2 g, 0.0181 mol) in anhydrous dimethylformamide (25 ml), then the resulting mixture is stirred for a further 6 hours at ambient temperature and left to stand overnight. The mixture is stirred into ice (200 g), made alkaline with postassium carbonate and extracted exhaustively with dichloromethane. The combined dichloromethane extracts are washed once with water (20 ml), dried over magnesium sulphate and concentrated by evaporation in vacuo. After recrystallization from ethyl acetate, colorless crystals (4.5 g) are obtained, mp. 199°-200° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04550107 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-83ad965268b6480bbafe7dcc759189d3 |
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| Source note | uspto-grants-1985_10 |
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