Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 69557664 | HCID 69557664 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 69557250 | HCID 69557250 | 95% |
Reaction Steps
A mixture of 67 mg (0.15 mmol) of [[5-(aminooxoacetyl)-6-ethyl-7-[(3-chlorophenyl)methyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl]oxy]acetic acid methyl ester and 2 mL of methanol were treated with 0.15 mL of 2 M sodium hydroxide and stirred at ambient temperature for 3 days. The reaction was concentrated to an oil then diluted with 5 mL of water. The product precipitated upon the addition of 0.45 mL of 1 M HCl to provide 59 mg (95%) of [[5-(aminooxoacetyl)-6-ethyl-7-[(3-chlorophenyl)methyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl]oxy]acetic acid as a white solid. nmr (500 MHz, dmso-d6) δ1.01 (t, J=7.4 Hz, 3H), 2.95 (q, J=7.4 Hz, 2H), 4.92 (s, 2H), 5.60 (s, 2H), 7.03 (d, J=7.4 Hz, 1H), 7.26 (s, 1H), 7.34 (m, 2H), 7.58 (br s, 1H), 8.00 (br s, 1H), 8.46 (s, 1H), 12.9 (br s, 1H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06384041B1 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-19d2d46a34dd46c0921dee469cc1d714 |
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| Source note | uspto-grants-2002_05 |
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