HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234795Generated: October 30, 2026
Dimethylformamide → HCID 178486368, compound
https://huagongshe.com/reaction/2234795
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 86612905 | HCID 86612905 | — |
| Product | HCID 178486368 | HCID 178486368 | — |
Reaction Steps
To a stirred solution of nucleoside 6.6 (10 mg, 0.030 mmol) in DMF (0.5 mL) was added N-bromosuccinimide (11.25 mg, 2.10 eq.) at 0° C. under argon. The reaction mixture was stirred at 0° C. for 1 hr then quenched with MeOH (0.5 mL). The mixture was evaporated to dryness and the residue was purified on a silica gel column with 5% MeOH in CH2C1 to give compound 14.1 as a mixture of diastereoisomers (8 mg, 65%). The isolated compound was characterized by 1H NMR, COSY, NOESY and LCMS. 1H NMR (300 MHz, DMSO-d6) δ 11.29 (s, 1H, NH), 8.54 (s, 1H, H-4), 8.00 (s, 1H, H-1), 6.24, 6.21 (2s, 1H, H-1′), 5.22-5.08 (m, 4H, 3×OH, H-8), 4.77-4.73 (m, 1H, H-9), 3.95-3.7 (m, 4H, H-3′, H-4′ 2×H-5′), 3.24, 3.21 (2s, 3H, OCH3), 0.68, 0.66 (2s, 3H, CH3). ES MS: 501.7 (+CH3COO−).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07713941B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-90f6063f1e9f4171a43eccd9c8816fc2 |
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| Source note | uspto-grants-2010_05 |
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