Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | alpha-Acetobromogalactose | HCID 2734143 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 51224-13-6 | HCID 86698937 | 91% |
Reaction Steps
2,3,4,6-tetra-O-acetyl-α-D-galactopyranosyl bromide (6; 15.00 g, 36.48 mmol) and thiourea (3.05 g, 40.07 mmol) were dissolved in acetone (75 mL). The solution was heated to reflux for 2 hours, and subsequently filtered and cooled to 20° C. Addition of pentane (75 mL) resulted in the precipitation of the product as a white, crystalline solid (16.11 g, 91%). 1H-NMR (400 MHz, [D6]DMSO,): δ=1.95 (s, 3H, CH3), 2.01 (s, 3H, CH3), 2.08 (s, 3H, CH3), 2.14 (s, 3H, CH3), 4.09 (m, 2H, H6, H6′), 4.45 (t, J=6.4 Hz, 1H, H5), 5.11 (t, J2,3=10 Hz, 1H, H2), 5.22 (dd, J2,3=9.9 Hz, J3,4=3.2 Hz, 1H, H3), 5.39 (d, J=3.2 Hz, 1H, H4), 5.71 (d, J1,2=10 Hz, 1H, H1), 9.11 (br, 2H, NH2), 9.35 (br, 2H, NH2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09427482B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-e453abe8ac3542b4985ced8e04094371 |
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| Source note | uspto-grants-2016_08 |
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