HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013331Generated: November 1, 2026
4-Methylmorpholine → 8-Tert-butyl-1-oxa-2-azaspiro[4.5]dec-2-ene-3-carboxylic acid-(4-tert-butylphenyl)amide
https://huagongshe.com/reaction/1013331
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | N-(4-(aminomethyl)-2-fluorophenyl)methanesulfonamide | HCID 21097526 | — |
| Reactant | 8-Tert-butyl-1-oxa-2-azaspiro[4.5]dec-2-ene-3-carboxylic acid | HCID 57951449 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 8-Tert-butyl-1-oxa-2-azaspiro[4.5]dec-2-ene-3-carboxylic acid-(4-tert-butylphenyl)amide | HCID 57951457 | — |
Reaction Steps
The compound 8-tert-butyl-1-oxa-2-azaspiro[4.5]dec-2-ene-3-carboxylic acid (120 mg, 0.51 mmol), N-(4-aminomethyl-2-fluorophenyl)methanesulphonamide (110 mg, 0.51 mmol), 4-methylmorpholine (101 mg, 1.02 mmol) and O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (288 mg, 0.65 mmol) (HBTU) were dissolved in DMF (10 ml) and stirred overnight under a nitrogen atmosphere at RT. The solvent was removed under vacuum, the residue taken up in EtOAc and sat. aq. NaHCO3 solution and the phases were separated. The aqueous phase was extracted several times with EtOAc and the combined organic phases were dried over magnesium sulphate and the solvent was removed under vacuum. After purification by column chromatography (silica gel, hexane/EtOAc 2:1), the desired product 8-tert-butyl-1-oxa-2-azaspiro[4.5]dec-2-ene-3-carboxylic acid-(4-tert-butylphenyl)amide was obtained as a trans isomer (30 mg, 13% of the theoretical amount) and cis isomer (100 mg, 45% of the theoretical amount).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07981883B2 |
|---|
| Source dataset | uspto-grants-2011_07 |
|---|
| ORD ID | ord-84f9cb16e3214dde8eef56ba9ad7ac7a |
|---|
| Source note | uspto-grants-2011_07 |
|---|