Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl isocyanate | HCID 8022 | — |
| Reactant | HCID 67204778 | HCID 67204778 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86715425 | HCID 86715425 | 15.3% |
Reaction Steps
A solution of (3aR,5R,6S,7R,7aR)-2-amino-5-(hydroxymethyl)-5,6,7,7a-tetrahydro-3aH-pyrano[3,2-d]thiazole-6,7-diol (100 mg, 0.45 mmol) in N,N-dimethylformamide (10 mL) was treated with isocyanatoethane (32 mg, 0.45 mmol) for 1 hour at room temperature. The reaction mixture was condensed to give a residue, which was purified by Prep-HPLC with the following conditions [(Prep-HPLC): Column, 19*150 mm; mobile phase, water with 0.03% NH3H2O and CH3CN (10% CH3CN up to 45% in 10 min); Detector, 220 nm] to give the title compound as a white solid (20 mg, 15%). (ES, m/z)[M+H]+291.9; 1H NMR (300 MHz, D2O) δ6.51-6.52 (d, J=6.3 Hz, 1H), 4.60-4.65 (m, 1H), 3.96-4.02 (t, J=9.0 Hz, 1H), 3.67-3.78 (m, 3H), 3.43-3.49 (t, J=9.6 Hz, 1H), 3.08-3.18 (m, 2H), 0.98-1.02 (t, J=7.2 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08927507B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-41162a586eec47768f715cf0adabe8e7 |
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| Source note | uspto-grants-2015_01 |
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