HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480774Generated: October 25, 2026
Dichloromethane → 5-amino-7-(methoxyacetyl)-5,7-dihydro-6H-dibenz[b,d]azepin-6-one hydrochloride
https://huagongshe.com/reaction/480774
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Bromomethyl acetate | HCID 68536 | — |
| Reactant | 5-(N-Boc-amino)-5,7-dihydro-6H-dibez[b,d]azepin-6-one | HCID 11493548 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-amino-7-(methoxyacetyl)-5,7-dihydro-6H-dibenz[b,d]azepin-6-one hydrochloride | HCID 22312635 | — |
Reaction Steps
A solution of 5-(N-Boc-amino)-5,7-dihydro-6H-dibenz[b,d]azepin-6-one (1.03, 3.08 mmol) (Example 7-E) in DMF was treated with Cs2CO3 (1.10 g, 3.39 mmol) and warmed to 60° C. To the reaction mixture was added bromomethyl acetate (0.321 ml, 3.39 mmol) (Aldrich) and stirring continued for 17 h. After cooling to 23° C. the mixture was diluted with CH2Cl2, washed with several portions of brine and dried over Na2SO4. The title compound was purified by chromatography (SiO2, CHCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06653303B1 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-f53dd6aabbf640279e24bf9b635ffcfa |
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| Source note | uspto-grants-2003_11 |
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