HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530626Generated: November 3, 2026
Methanamine, N-methoxy-, hydrochloride (1:1) → Tert-butyl 3-[methoxy(methyl)carbamoyl]pyrrolidine-1-carboxylate
https://huagongshe.com/reaction/1530626
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-((Tert-butoxy)carbonyl)pyrrolidine-3-carboxylic acid | HCID 2760529 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl 3-[methoxy(methyl)carbamoyl]pyrrolidine-1-carboxylate | HCID 57419605 | 106% |
Reaction Steps
A mixture of 1-(tert-butoxycarbonyl)pyrrolidine-3-carboxylic acid (5.0 g, 23 mmol), O,N-dimethylhydroxylamine hydrochloride (4.51 g, 46.5 mmol), DIPEA (9.00 g, 69.6 mmol), and HATU (17.6 g, 46.5 mmol) in DMF (50 mL) was stirred at 15° C. for 16 h. DMF was removed, the residue was extracted with ethyl acetate, washed with brine, dried over MgSO4, filtered, and evaporated to give the crude product, which was purified by silica gel chromatography eluting with a 0-30% gradient of EtOAc in petroleum ether to afford tert-butyl 3-(N-methoxy-N-methylcarbamoyl)pyrrolidine-1-carboxylate (6.3 g, 90% yield) as pale yellow oil. LCMS (ESI) m/z: 203.2 [M-56+H+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09090628B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-7fba2dc770e94740ac687223fb0c1ff3 |
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| Source note | uspto-grants-2015_07 |
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