HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712275Generated: November 4, 2026
O-Methylhydroxylamine hydrochloride → HCID 87222433, compound
https://huagongshe.com/reaction/712275
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | Ethyl 1-[5-[7-acetyl-2-(ethylcarbamoylamino)-1,3-benzothiazol-5-yl]pyrimidin-2-yl]-4-methyl-piperidine-4-carboxylate | HCID 86663987 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 87222433 | HCID 87222433 | — |
Reaction Steps
O-Methyl hydroxylamine hydrochloride (64 mg, 0.784 mmol) was added to ethyl 1-[5-[7-acetyl-2-(ethylcarbamoylamino)-1,3-benzothiazol-5-yl]pyrimidin-2-yl]-4-methyl-piperidine-4-carboxylate (200 mg, 0.39 mmol) in DMF (5 mL). The reaction mixture was heated to 60° C. for 4 h after which time LCMS indicated clean conversion to the desired product. The reaction was diluted with EtOAc, washed with water then brine and the organic layer dried (MgSO4), filtered and the solvent removed in vacuo. The crude product obtained was used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181234B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-11fe1b5aad664f1382a5c5a780db6bbe |
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| Source note | uspto-grants-2015_11 |
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