HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828666Generated: November 1, 2026
4-Methylmorpholine → HCID 131725786, compound
https://huagongshe.com/reaction/1828666
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Phenacylamine | HCID 11952 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | Biotin | HCID 171548 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131725786 | HCID 131725786 | 72% |
Reaction Steps
The D-biotin (1 g, 4.1 mmol) is solubilized in 45 ml of anhydrous DMF in the hot state. The mixture is cooled to 0° C. under argon, and then N-methylmorpholine (590 μl, 5.33 mmol) and isobutyl chloroformate (840 μl, 6.60 mmol) are successively added. The mixture is kept stirred for 30 min, and then 2-aminoacetophenone (824 mg, 6.10 mmol) is added. The solution is maintained stirred at room temperature for 3 h 30 min, and then evaporated to dryness. The residue is taken up in 50 ml of water. The precipitate obtained is filtered, washed with water and then with 50 ml of MeOH in the hot state. The precipitate obtained is filtered and washed with water. Recrystallization is carried out by dissolving the product in MeOH in the hot state and reprecipitating by addition of water. The precipitate is filtered, washed with water, and then with ether to give 1.1 g (2.95 mmol, 72%) of crude product 1c.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07060441B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-d7fe3c19e3a64e71ba7db7461fdc5008 |
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| Source note | uspto-grants-2006_06 |
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