Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 69840849 | HCID 69840849 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 55299026 | HCID 55299026 | — |
Reaction Steps
tert-Butyl-(3R)-3-{[(methylamino)carbonyl]amino}pyrrolidine-1-carboxylate 6-3 (2.174 g, 8.93 mmol) was dissolved in 3 mL CH2Cl2 and the solution was cooled to 0° C. 4.0M HCl in dioxane (33.50 mL, 134.0 mmol) was added and the solution was allowed to warm to room temperature. After 4.5 hours the reaction was concentrated in vacuo to afford N-methyl-N′-[(3R)-pyrrolidin-3-yl]urea 6-4 as an off-white solid. HCl salt: 1H NMR (DMSO-d6) δ 9.13 (bs, 2H), 4.15 (m, 1H), 3.10-3.3.29 (m, 3H), 2.96-2.87 (m, 1H), 2.54 (s, 3H), 2.13-2.01 (m, 1H), 1.75 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06875767B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-c47701152c404aca8d6a5b75c826457d |
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| Source note | uspto-grants-2005_04 |
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