HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575465Generated: October 30, 2026
Ammonium Hydroxide → HCID 86693530, compound
https://huagongshe.com/reaction/575465
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 86693528 | HCID 86693528 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86693530 | HCID 86693530 | — |
Reaction Steps
A solution of ethyl 9-iodo-5H-spiro[benzo[b]pyrazolo[1,5-d][1,4]oxazepine-4,1′-cyclopropane]-2-carboxylate (313 mg, 0.76 mmol) in ammonium hydroxide (3 mL) and dioxane (2 mL) was sealed in a 20 mL microwave vial and heated at 110° C. behind a blast shield. The mixture was cooled to room temperature, diluted with ethyl acetate and water and washed with sodium bicarbonate solution. The organics were dried over sodium sulfate and concentrated by rotoevaporation to give the titled compound which was used without purification in subsequent operations. 1H NMR (400 MHz, DMSO) δ 8.44 (d, J=2.1 Hz, 1H), 7.83 (br s, 1H), 7.61 (dd, J=8.5, 2.2 Hz, 1H), 7.33 (br s, 1H), 6.99 (d, J=8.5 Hz, 1H), 6.55 (s, 1H), 4.22 (s, 2H), 1.10-0.96 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09034866B2 |
|---|
| Source dataset | uspto-grants-2015_05 |
|---|
| ORD ID | ord-c858523e52984d49a05ced712dc61c54 |
|---|
| Source note | uspto-grants-2015_05 |
|---|