HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470323Generated: October 30, 2026
Phosphorus oxychloride → HCID 53486023, compound
https://huagongshe.com/reaction/470323
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178487123 | HCID 178487123 | — |
| Reactant | 5,6-Dihydrobenzo[h]quinazolin-2-ol | HCID 178517548 | — |
| Product | HCID 53486023 | HCID 53486023 | 86% |
Reaction Steps
A suspension of 8-Methoxy-5,6-dihydro-benzo[h]quinazolin-2-ol as a 1:1 urea complex from preparation 1 (20 g, 69.0 mM) in POCl3 (350 ml) was heated under nitrogen atmosphere at 100° C. for 20 hr. The POCl3 was removed under reduced pressure and the residue was suspended in dichloromethane (300 ml) and cooled in an ice bath and then concentrated sodium bicarbonate (500 ml) was carefully added followed by 1 N NaOH (200 ml) and the phases separated. The aqueous phase was extracted with dichloromethane (3×500 ml) and the pooled organic phases were dried over Na2SO4, filtered and the filtrate evaporated under reduced pressure to give 2-Chloro-8-methoxy-5,6-dihydro-benzo[h]quinazoline (2, 14.46 g, 86% yield) as a yellow solid. ES-MS MH+ 247.1. 1H NMR (300 MHz, ppm, DMSO-d6): 8.54 (s, 1H), 8.09 (d, 1H), 6.99 (m, 3H) 3.84 (s, 3H), 2.91 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08629147B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-531113abc9c748c99e32a93996247292 |
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| Source note | uspto-grants-2014_01 |
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