HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464582Generated: October 29, 2026
Phosphorus oxychloride → 1,9-Dichloro-3-methyl-7-phenyl-5H-pyrimido[4,5-d][2]benzazepine
https://huagongshe.com/reaction/464582
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 135759068 | HCID 135759068 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,9-Dichloro-3-methyl-7-phenyl-5H-pyrimido[4,5-d][2]benzazepine | HCID 13271791 | — |
Reaction Steps
A solution of 3.5 g (10.4 mmol) of 9-chloro-3-methyl-7-phenyl-5H-pyrimido[4,5-d][2]benzazepin-1(2H)-one and 22 mL of phosphorous oxychloride in 100 mL of methylene chloride was stirred at room temperature for 18 hr. The reaction mixture was concentrated at reduced pressure to a solid residue. The residue was partitioned between ice cold saturated aqueous sodium bicarbonate and methylene chloride. The methylene chloride solution was dried over anhydrous sodium sulfate and concentrated at reduced pressure to a yellow residue. Purification by column chromatography (silica gel, 40.0 g; eluent: methylene chloride ether, 10:1) gave a pale yellow solid, mp 190°-192°. A portion was recrystallized from a mixture of ether and petroleum ether to yield colorless prisms, mp 191°-193°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04548750 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-6ec5225e67dc42d79295a7e2dac6e47f |
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| Source note | uspto-grants-1985_10 |
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