HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222733Generated: October 29, 2026
Oxane-4-carboxylic acid → HCID 10320019, compound
https://huagongshe.com/reaction/222733
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxane-4-carboxylic acid | HCID 219302 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | HCID 10244844 | HCID 10244844 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10320019 | HCID 10320019 | — |
Reaction Steps
Tetrahydro-pyran-4-carboxylic acid (252 mg, 1.94 mmol), 1-hydroxy benzotriazole hydrate (262 mg, 1.94 mmol) and N-cyclohexylcarbodiimide N′-methyl polystyrene (1.7 mmol/g, 2.3 g, 3.88 mmol) were stirred at room temperature in dichloromethane (10 ml) for 15 minutes. 6-[(3-Cyclobutyl-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl)oxy]-3-pyridinamine (E236) (300 mg, 0.97 mmol) was added and stirring continued for 16 hours. The reaction mixture was applied to a SCX ion exchange cartridge (Varian bond-elute, 5 g) and washed with methanol and then a mixture of 0.880 ammonia/methanol. The combined basic fractions were concentrated in vacuo and the resulting residue was purified by column chromatography eluting with a mixture of 0.880 ammonia:methanol:dichloromethane (0.5:4.5:95) to afford the title product (E241); MS (ES+) m/e 422 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207331B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-6f96cfd327ce444085ee99500cc1dfea |
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| Source note | uspto-grants-2012_06 |
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