Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 20718797 | HCID 20718797 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18326593 | HCID 18326593 | — |
Reaction Steps
(−)-4-(3,4-Difluorophenyl)-3,6-dimethyl-2-oxo-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid methyl ester (650 mg, 2.19 mmol) was dissolved in methanol (10 ml), treated with 2.5N sodium hydroxide (10 ml), and warmed to 500° C. for 8hr. The solvent was removed in vacuo, the remaining aqueous phase treated with 10% KHSO4 (aq), and extracted with ethyl acetate (3X). The extracts were combined, washed with brine, dried over magnesium sulfate, filtered and concentrated to dryness in vacuo to give a crude oil. Crystallization from diethyl ether gave the product as a white solid [αD]=−128°, c=0.20 MeOH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06339090B1 |
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| Source dataset | uspto-grants-2002_01 |
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| ORD ID | ord-efe52d08990148af8201c6b401dc19ea |
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| Source note | uspto-grants-2002_01 |
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