HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Ethylhexylamine → HCID 178443603, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Ethylhexylamine | HCID 7719 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178432852 | HCID 178432852 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178443603 | HCID 178443603 | 63% |
Reaction Steps
This compound was prepared according to the method described in Example 2 by employing 4-chloro-2-methyl-6-phenylpyrrolo[3,2-d]pyrimidine (Example 1(e)) (70.0 mg, 0.29 mmol), 2-ethylhexylamine (Aldrich Chemical Company) (0.24 mL, 1.44 mmol) and K2CO3 (0.40 g, 2.87 mmol) in H2O (2 mL) to give 61 mg (63%) of the title compound as a white solid. An analytical sample was obtained by recrystallization from i-PrOH. Mp: 288-289° C. (dec.). 1H NMR (CDCl3; 500 MHz): δ 0.72-0.78 (m, 6), 1.15-1.34 (m, 9), 2.62 (s, 3), 3.56 (dd, 2, J=5.3, 7.6), 6.71 (s, 2), 7.17-7.24 (m, 3), 7.59 (d, 2, J=7.6), 12.78 (br s, 1). MS m/z: 337 (M+1), 335 (M−1). HRMS: Calcd for M+H: 337.2392. Found: 337.2397.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06187777B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-024d5be90d9c4a2eb11be3eb3f2cfa2b |
| Source note | uspto-grants-2001_02 |