Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Benzyl 3-(chlorosulfonyl)pyrrolidine-1-carboxylate | HCID 53229936 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66698120 | HCID 66698120 | 69% |
Reaction Steps
Methylamine (40 wt % in H2O, 1 mL) was added to a solution of 3-chlorosulfonyl-pyrrolidine-1-carboxylic acid benzyl ester (256 mg, 0.843 mmol) in THF (1 mL) at 0° C. The mixture was stirred at 0° C. for 10 min, and then warmed to room temperature and stirred for 2 hrs. Water was added and the phases were separated. The aqueous phase was extracted with CH2Cl2 (2×), the combined organic extracts were dried (Na2SO4), and the solvent was removed under vacuum. Chromatography on neutral alumina, eluting with CH2Cl2/MeOH (99:1 to 95:5), gave benzyl 3-[(methylamino)sulfonyl]-1-pyrrolidinecarboxylate (173 mg, 69%): 1H NMR (CDCl3) δ 7.36-7.29 (m, 5H), 5.14 (d, J=1.9 Hz, 2H), 4.27 (d, J=42.6 Hz, 1H), 3.80-3.70 (m, 4H), 3.50 (m, 1H), 2.82 (d, J=4.9 Hz, 3H), 2.35 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108980B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-e0f70c2605444749bc986ed4640fff21 |
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| Source note | uspto-grants-2015_08 |
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