HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828664Generated: October 30, 2026
3'-Aminoacetophenone → HCID 131725786, compound
https://huagongshe.com/reaction/1828664
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3'-Aminoacetophenone | HCID 7417 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | Biotin | HCID 171548 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131725786 | HCID 131725786 | 70% |
Reaction Steps
The D-biotin (1.0 gram (g), 4.1 millimoles (mmol) is solubilized in 45 milliliters (ml) of anhydrous DMF in the hot state. The mixture is cooled to 0° C. under argon, and then N-methylmorpholine (590 microliters (μl), 5.33 mmol) and isobutyl chloroformate (840 μl, 6.60 mmol) are successively added. The mixture is kept stirred for 30 minutes (min), and then 3-aminoacetophenone (824 mg, 6.10 mmol) and N-methylmorpholine (480 μl, 4.35 mmol) in 10 ml of DMF are added. The solution is maintained stirred at 0° C. for 2 hours (h), and then evaporated to dryness. The residue is taken up in 3 ml of MeOH, and then 50 ml of water are added. The precipitate obtained is filtered, washed with water, CH2Cl2 and ether to give 1.2 g (80%) of crude product 1a. Recrystallization from the MeOH—H2O pair gives 1a (1.01 g, 70%) in the form of a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07060441B2 |
|---|
| Source dataset | uspto-grants-2006_06 |
|---|
| ORD ID | ord-72d62933a61e49249fdea47ca84701a5 |
|---|
| Source note | uspto-grants-2006_06 |
|---|