Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | Pyrimidine,5-[(1E)-2-(3R)-3-pyrrolidinylethenyl]- | HCID 11528435 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86659301 | HCID 86659301 | — |
Reaction Steps
(R)-5-((E)-2-pyrrolidin-3-ylvinyl)pyrimidine free base (189 mg, 1.077 mmol, freshly prepared) was dissolved in acetonitrile (5 ml). The solution was then treated with 1.1 eq. of an maleic acid solution (1M in tetrahydrofuran) at ambient temperature. The mixture was warmed up to 50° C. and cooled down slowly to ambient temperature overnight. The solid obtained was filtered and dried under suction before being analysed by XRPD, and 1H-NMR. The XRPD diffractogram of (R)-5-((E)-2-pyrrolidin-3-ylvinyl)pyrimidine mono-maleate Form I is shown in FIG. 7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145396B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-0928959bca6f46e890b889f912bb8aa6 |
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| Source note | uspto-grants-2015_09 |
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