HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624216Generated: October 26, 2026
N-Methylbenzylamine → N-(4-{[benzyl(methyl)amino]methyl}phenyl)-1,3-dihydro-2H-isoindole-2-carboxamide
https://huagongshe.com/reaction/624216
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Methylbenzylamine | HCID 7669 | — |
| Reactant | 1-Methylpyrrolidine | HCID 8454 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Isoindoline | HCID 422478 | — |
| Reactant | 4-(Chloromethyl)phenyl isocyanate | HCID 2733319 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-(4-{[benzyl(methyl)amino]methyl}phenyl)-1,3-dihydro-2H-isoindole-2-carboxamide | HCID 57510227 | — |
Reaction Steps
A suspension of isoindoline (0.1 g, 0.839 mmol) and N-ethyl-N-isopropylpropan-2-amine (0.219 ml, 1.259 mmol) in acetonitrile (2.80 ml) was treated with N-methylpyrrolidine (2.80 ml). The solution was cooled to 0° C. and 1-(chloromethyl)-4-isocyanatobenzene (0.155 g, 0.923 mmol) was added. After stirring for 2 hours at 0° C., the reaction was treated with a solution of N-methyl-1-phenylmethanamine (0.102 g, 0.839 mmol) in 0.5 mL acetonitrile. The reaction was stirred at 0° C. for 5 minutes and at ambient temperature for 30 minutes. The reaction was treated with water and the mixture was stirred for 4 hours. The suspension was filtered and the solid collected was washed with water and dried under vacuum to provide the title compound. 1H NMR (300 MHz, DMSO-d6) δ ppm 8.31 (s, 1H), 7.56-7.49 (m, 2H), 7.40-7.28 (m, 8H), 7.27-7.19 (m, 3H), 4.76 (bs, 4H), 3.47 (s, 2H), 3.43 (s, 2H), 2.06 (s, 3H); MS (ESI(+)) m/e 372 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09302989B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-e6061dde516c4a0f8f3a882e62e74067 |
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| Source note | uspto-grants-2016_04 |
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