HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441374Generated: October 31, 2026
Methylamine → (R)-1-(4-Nitro-phenyl)-pyrrolidine-2-carboxylic acid methylamide
https://huagongshe.com/reaction/1441374
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 1-(4-Nitrophenyl)-D-proline | HCID 26201931 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (R)-1-(4-Nitro-phenyl)-pyrrolidine-2-carboxylic acid methylamide | HCID 68688348 | — |
Reaction Steps
To (R)-1-(4-Nitro-phenyl)-pyrrolidine-2-carboxylic acid (Method 55; 1.8 g, 7.6 mmol) in DCM (50 ml) was added HATU (3.2 g, 8.4 mmol) and DIPEA (2.0 ml, 11.4 mmol). The reaction was stirred for 10 minutes before the addition of methylamine (2.0 N in THF, 5.0 ml, 15 mmol); the reaction was stirred for 1 hour before being quenched with water (50 ml). The reaction was extracted with DCM (3×100 ml), dried and solvent removed in vacuo to yield a yellow gum. Purification was achieved via column chromatography eluting with 20% EtOAc/isohexane, 60% EtOAc/isohexane and finally 100% EtOAc. The title compound was obtained as an orange gum; (1.4 g, 74%). NMR (299.954 MHz, CDCl3) 8.10 (d, 2H), 6.56 (d, 2H), 6.24 (s, 1H), 4.20 (t, 1H), 3.75 (t, 1H), 3.40 (q, 1H), 2.80 (d, 3H), 2.36-2.29 (m, 2H), 2.13-2.05 (m, 2H); m/z 250.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07655652B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-95cd04268cbe4dee89809271533fad8a |
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| Source note | uspto-grants-2010_02 |
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