HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615219Generated: October 26, 2026
4-(2,3-epoxypropoxy)-N-methylbenzamide → 1-[N-[2-(2,3-dihydro-2,2-dimethyl-4-oxo-4H-1,3-benzoxazin-6-yloxy)-1-methylethyl]benzylamino]-3-(4-methylcarbamoylphenoxy)propan-2-ol
https://huagongshe.com/reaction/615219
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(2,3-epoxypropoxy)-N-methylbenzamide | HCID 12238248 | — |
| Reactant | 6-(2-benzylaminopropoxy)-2,3-dihydro-2,2-dimethyl-4H-1,3-benzoxazin-4-one | HCID 13754414 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-[N-[2-(2,3-dihydro-2,2-dimethyl-4-oxo-4H-1,3-benzoxazin-6-yloxy)-1-methylethyl]benzylamino]-3-(4-methylcarbamoylphenoxy)propan-2-ol | HCID 54394708 | — |
Reaction Steps
A solution of 13.6 g of 6-(2-benzylaminopropoxy)-2,3-dihydro-2,2-dimethyl-4H-1,3-benzoxazin-4-one and 10.4 g of 4-(2,3-epoxypropoxy)-N-methylbenzamide in 80 ml of isopropanol is refluxed for 30 hours. The residue remaining after the solvent has been evaporated off is divided between ether and 2N hydrochloric acid. The acidic, aqueous phase is separated off, and, whilst cooling with ice, rendered alkaline with approximately 10% aqueous ammonia solution and extracted with ethyl acetate. By separating off, drying (MgSO4) and concentrating the ethyl acetate extract by evaporation, the crude 1-[N-[2-(2,3-dihydro-2,2-dimethyl-4-oxo-4H-1,3-benzoxazin-6-yloxy)-1-methylethyl]benzylamino]-3-(4-methylcarbamoylphenoxy)propan-2-ol is obtained as an oil which may be used without further purification for catalytic debenzylation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04497813 |
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| Source dataset | uspto-grants-1985_02 |
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| ORD ID | ord-3f60ceb6a00a458a859a5d314196c66b |
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| Source note | uspto-grants-1985_02 |
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