Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 67709598 | HCID 67709598 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86751446 | HCID 86751446 | — |
Reaction Steps
2.9 g (9 mmol) of (1-(3-aminopropyl)-3-(methoxycarbonylphenylmethyl)ureido)acetic acid trifluoroacetate are dissolved in 50 ml of methanol. After cooling down to 0° C., 1.34 g (11 mmol) of thionyl chloride are slowly added dropwise. The mixture is allowed to warm up to room temperature, then stirred overnight, concentrated and crystallized by adding ethyl acetate and methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05681838 |
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| Source dataset | uspto-grants-1997_10 |
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| ORD ID | ord-e46e46b56ba8417d9aa6e9d5861146f8 |
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| Source note | uspto-grants-1997_10 |
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