HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548681Generated: October 29, 2026
Ammonium formate → HCID 15949402, compound
https://huagongshe.com/reaction/548681
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 15949316 | HCID 15949316 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 15949402 | HCID 15949402 | — |
Reaction Steps
Ammonium formate (122 mg, 1.9 mmol) was added in one portion to a solution of 3-[(8-chloro-2,3-dimethyl-4-oxo-3,4-dihydro-2H-1,3-benzoxazin-7-yl)oxy]-5-{[(1S)-1-methyl-2-(methyloxy)ethyl]oxy}-N-(1-methyl-1H-pyrazol-3-yl)benzamide (100 mg, 0.19 mmol) in ethanol (3 mL). The reaction was blanketed with argon and 10% palladium on carbon (20 mg) was added. The mixture was heated to 140° C. for 10 minutes in a Smith Creator microwave after which complete conversion to desired product was observed. The reaction mixture was filtered through diatomaceous earth and the filter pad was washed well with ethyl acetate. The filtrate was evaporated in vacuo and the residue purified by column chromatography on silica, eluting with 60-100% ethyl acetate in hexanes, and then by chromatography on alumina, eluting with 20-60% ethyl acetate in hexanes, to afford the title compound as a colourless oil which foamed under high vacuum (50 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07943607B2 |
|---|
| Source dataset | uspto-grants-2011_05 |
|---|
| ORD ID | ord-966c6920b7d348c8af6a7dbe3fd105e8 |
|---|
| Source note | uspto-grants-2011_05 |
|---|