HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004004Generated: October 31, 2026
Phosphorus oxychloride → 5-Benzyloxy-4-methoxy-2-{1-[4-(morpholinecarbonyl)-1,4-diazepan-1-yl]ethylideneamino}benzonitrile
https://huagongshe.com/reaction/1004004
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 2-Amino-5-(benzyloxy)-4-methoxybenzonitrile | HCID 11075994 | — |
| Reactant | 1-Acetyl-4-(4-morpholinecarbonyl)-1,4-diazepane | HCID 15538286 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Benzyloxy-4-methoxy-2-{1-[4-(morpholinecarbonyl)-1,4-diazepan-1-yl]ethylideneamino}benzonitrile | HCID 53652588 | — |
Reaction Steps
Phosphorous oxychloride (0.81 ml, 0.0086 mol) was added to a solution of 1-acetyl-4-(4-morpholinecarbonyl)-1,4-diazepane (4.02 g, 0.0157 mol) in dichloromethane (25 ml) and the mixture stirred for 30 minutes at room temperature. A solution of 2-amino-5-benzyloxy-4-methoxybenzonitrile (2 g, 0.0078 mol) in dichloromethane (25 ml) was then added and the reaction stirred for 18 hours at 40° C. On cooling, the reaction mixture was poured carefully in to ice/water (100 ml) and extracted with dichloromethane (2×100 ml). The combined organic layers were dried (MgSO4), filtered and evaporated under reduced pressure to give a brown oil. The crude product was purified on silica gel eluting with a solvent gradient of methanol:dichloromethane (2:98 to 10:90 v/v) to give the subtitle compound. Rf 0.67 (0.880 aqueous ammonia:methanol:dichloromethane 1:7:92, v/v). MS m/z 492 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06048864 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-d8aaa0f43adb45a0b7c0fecc857d8356 |
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| Source note | uspto-grants-2000_04 |
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