HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351849Generated: October 26, 2026
Dimethyl-p-toluidine → 2-Chloro-4-(2,4-dimethoxy-benzyl)-7-methylsulfanyl-3,4-dihydro-benzo[e][1,4]diazepin-5-one
https://huagongshe.com/reaction/351849
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl-p-toluidine | HCID 7471 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 4-(2,4-Dimethoxy-benzyl)-7-methylsulfanyl-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione | HCID 22713482 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Chloro-4-(2,4-dimethoxy-benzyl)-7-methylsulfanyl-3,4-dihydro-benzo[e][1,4]diazepin-5-one | HCID 22713484 | — |
Reaction Steps
4-(2,4-Dimethoxy-benzyl)-7-methylsulfanyl-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione (630 mg, 1.7 mmol) and N,N-dimethyl-p-toluidine (489 μL, 3.4 mmol) were mixed in toluene (5 mL) and heated to 100° C. Then phosphorus oxychloride (170 μL, 1.9 mmol) was added dropwise and heating at 100° C. was continued for 1 h. The resulting dark red solution was used directly in the subsequent step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06743789B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-be20683897304400a6363b07e996b88e |
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| Source note | uspto-grants-2004_06 |
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