HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661723Generated: November 2, 2026
N,N-Diacetyl-O-methylhydroxylamine → HCID 74020018, compound
https://huagongshe.com/reaction/661723
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Diacetyl-O-methylhydroxylamine | HCID 538412 | — |
| Reactant | HCID 72794471 | HCID 72794471 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 74020018 | HCID 74020018 | 92% |
Reaction Steps
To a solution of 5-[(2-amino-ethoxyimino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide (8.14 mg, 0.02 mmol) described in Example 22 in a mixture of dimethylformamide (1 ml) and methanol (5 ml), N-methoxy-diacetamide (100 mg, 0.76 mmol) was added, and the mixture was stirred at room temperature for 14 hours. After completion of the reaction, the solvent was distilled off under reduced pressure, and the resulting residue was purified with Mega Bond Elut silica gel (5 g, Varian, Inc.). From the fractions eluted with 6% methanol/methylene chloride, 5-[(2-acetylamino-ethoxyimino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide (8.10 mg, 92% yield) was obtained as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08084645B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-d87d60022c124b60b620cc8f85240824 |
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| Source note | uspto-grants-2011_12 |
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