HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 11538279, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 24829100 | HCID 24829100 | — |
| Reactant | HCID 86634683 | HCID 86634683 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 11538279 | HCID 11538279 | 109.3% |
| Product | Ammonia methanol | HCID 21705897 | — |
Reaction Steps
A solution of 7-benzyl-6-chloro-7,9-dihydropurin-8-one (0.015 g, 0.075 mmol), C-[4-(4-chlorophenyl)piperidin-4-yl]methylamine bis hydrochloride (0.025 g, 0.085 mmol) and triethylamine (0.11 mL, 0.85 mmol) in n-butanol (0.5 mL) was heated at 150° C. in a microwave reactor for 3 h. The cooled mixture was partitioned between ethyl acetate (30 mL) and water (5 mL) and the organic layer was dried, filtered and concentrated. Purification on SCX-II acid resin, eluting with methanol then 1M ammonia/methanol, gave 6-[4-aminomethyl-4-(4-chlorophenyl)piperidin-1-yl]-7-ethyl-7,9-dihydropurin-8-one as a cream solid (0.016 g, 0.041 mmol, 56%). LC-MS (LCT2) m/z 387 [M+H+], Rt 4.18 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09006430B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-8cb1fb09341f4d108600efb00d57ec88 |
| Source note | uspto-grants-2015_04 |