HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Pyrrolidinepropanamine → HCID 22594099, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Pyrrolidinepropanamine | HCID 31670 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 22594113 | HCID 22594113 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 22594099 | HCID 22594099 | — |
Reaction Steps
A mixture of 4-[5-(3-dimethylaminobenzamido)-2-methylanilino]-6-chloropyrimidine (0.114 g), 3-pyrrolidin-1-ylpropylamine (0.95 ml), N,N-di-isopropylethylamine (0.063 ml) and n-butanol (2 ml) was stirred and heated to reflux for 18 hours. The mixture was evaporated and the residue was purified by column chromatography on silica using a 10:1 mixture of ethyl acetate and methanol as eluent. There was thus obtained the title compound (0.124 g); NMR Spectrum: (DMSOd6) 1.59 (m, 6H), 2.15 (s, 3H), 2.34 (m, 6H), 2.93 (s, 6H), 3.14 (m, 2H), 6.72 (m, 1H), 6.89 (m, 1H), 7.2 (m, 4H), 7.3 (m, 1H), 7.5 (m, 1H), 7.72 (m, 1H), 7.96 (m, 1H), 8.16 (s, 1H), 10.02 (s, 1H); Mass Spectrum: M+H+ 474.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06846827B1 |
| Source dataset | uspto-grants-2005_01 |
| ORD ID | ord-e5cbc5afa82e46fdbb07f13472749b0c |
| Source note | uspto-grants-2005_01 |