HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Naphthalenecarboxaldehyde → HCID 49855398, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Naphthalenecarboxaldehyde | HCID 6201 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 2-[6-(aminomethyl)-3-azabicyclo[3.1.0]hex-3-yl]pyrimidine-5-carboxylate | HCID 49857516 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 49855398 | HCID 49855398 | — |
Reaction Steps
Ethyl 2-[6-(aminomethyl)-3-azabicyclo[3.1.0]hex-3-yl]pyrimidine-5-carboxylate (200 mg, 0.76 mmol) was stirred with 2-naphthaldehyde (119 mg, 0.76 mmol) in MeOH (10 ml) at r.t. under N2 for 16 h. NaBH4 (46 mg, 1.22 mmol) was then added and the mixture stirred for 10 min. Sat. aq. NH4Cl (20 ml) was added and the mixture stirred for 20 min. The reaction was then diluted with H2O (50 ml) and extracted with Et2O (2×100 ml). The combined organic layers were dried (MgSO4) and the solvent removed in vacuo to give the title compound as a yellow oil which was used in the next step without further purification. LCMS purity 92%, m/z 403 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07932246B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-8de67212087f4628bed91103e0b3d2c3 |
| Source note | uspto-grants-2011_04 |