HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663164Generated: October 26, 2026
Water → N-(4-Chloro-benzyloxy)-2-(4-cyano-benzylamino)-benzamide
https://huagongshe.com/reaction/1663164
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Hydroxylamine, O-((4-chlorophenyl)methyl)-, hydrochloride (1:1) | HCID 217573 | — |
| Reactant | 4-(2,4-Dioxo-4H-benzo[d][1,3]oxazin-1-ylmethyl)-benzonitrile | HCID 58989817 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(4-Chloro-benzyloxy)-2-(4-cyano-benzylamino)-benzamide | HCID 58989877 | — |
Reaction Steps
To a stirred mixture of 4-(2,4-dioxo-4H-benzo[d][1,3]oxazin-1-ylmethyl)-benzonitrile (Preparation 7D, 319 mg) and O-(4-chloro-benzyl)-hydroxylamine hydrochloride (preparation 9, 267 mg) in DMF (10 ml) was added N-ethyldiisopropylamine (0.4 ml). The reaction mixture was heated to 100° C. and stirred for 17 hours. The mixture was cooled to room temperature and water was added. The pale brown precipitated material was isolated by filtration and re-crystallised from ethanol and gave the title compound as a white solid material. 13C-NMR (DMSO-d6) δ 148.2, 145.9, 135.1, 132.8, 132.5, 132.3, 130.6, 128.2, 128.0, 127.7, 118.8, 114.8, 113.2, 111.4, 109.5, 75.9, 45.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08034811B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-d224d29eec114b578e4bb08fbcd6d169 |
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| Source note | uspto-grants-2011_10 |
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