HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Diiodobenzene → (R)-1-(4-iodophenyl)-N,N-dimethylpyrrolidin-3-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Diiodobenzene | HCID 12208 | — |
| Reactant | (3R)-(+)-3-(Dimethylamino)pyrrolidine | HCID 2758521 | — |
| Reactant | 1-(4-Bromophenyl)-cis-3,5-dimethylpiperazine | HCID 66730361 | — |
| Product | (R)-1-(4-iodophenyl)-N,N-dimethylpyrrolidin-3-amine | HCID 66730449 | — |
Reaction Steps
The title compound was synthesized according to the synthesis of 1-(4-bromophenyl)-cis-3,5-dimethylpiperazine, except reacting 1,4-diiodobenzene (2.41 g, 7.30 mmol) with (R)—N,N-dimethylpyrrolidin-3-amine (1.0 g, 8.8 mmol). The title compound was purified by silica gel chromatography (MeOH/CH2Cl2, 2:98 to 12:88) as a yellow solid (1.17 g, 51%). 1H NMR (400 MHz, MeOD) δ 7.42 (d, J=8.2 Hz, 2H), 6.39 (d, J=8.0 Hz, 2H), 3.51-3.47 (m, 1H), 3.44-3.39 (m, 1H), 3.29-3.24 (m, 1H), 3.13-3.09 (m, 2H), 3.00-2.87 (m, 1H), 2.35 (s, 6H), 2.35-2.26 (m, 1H), 1.96-1.86 (m, 1H); MS ESI 317.0 [M+H]+, calcd for [C12H17IN2+H]+ 317.04.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08481533B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-57b08ec44a534953acdd55626e34bd64 |
| Source note | uspto-grants-2013_07 |