HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533194Generated: October 29, 2026
Boron tribromide → HCID 178520893, compound
https://huagongshe.com/reaction/533194
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 2-((5-(benzyloxymethyl)-4-methoxy-5H-pyrrolo[3,2-d]pyrimidin-7-yl)methylamino)-2-(hydroxymethyl)propane-1,3-diol | HCID 25223286 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ammonium Hydroxide | HCID 14923 | — |
| Product | HCID 178520893 | HCID 178520893 | 70.1% |
Reaction Steps
Boron tribromide (1 mL, 1.0 mmol) was added dropwise to a solution of 2-((5-(benzyloxymethyl)-4-methoxy-5H-pyrrolo[3,2-d]pyrimidin-7-yl)methylamino)-2-(hydroxymethyl)propane-1,3-diol (30 mg, 74.5 μmol) in dichloromethane (5 mL) and stirred at r.t. A white solid precipitated from the reaction after 1 h and the reaction was then quenched with methanol, concentrated in vacuo and co-distilled with methanol (3×25 mL) to afford a crude residue. The residue was dissolved in methanol absorbed onto silica and chromatographed eluting with 5:4.5:0.5 DCM:MeOH:NH4OH to afford 2-((4-hydroxy-5H-pyrrolo[3,2-d]pyrimidin-7-yl)methylamino)-2-(hydroxymethyl)propane-1,3-diol (7 mg, 26.1 μmol, 35.0% yield) as a white solid which was converted to the HCl salt for NMR analysis. Mpt 223-224° C. (plates from EtOH). 1H NMR (D2O, referenced to internal acetone at 2.225 ppm) δ 9.06, (s, 1H), 7.92 (s, 1H), 4.59 (s, 2H), 3.91 (s, 6H). 13 NMR (D2O, referenced to internal acetone at δ 31.5) δ 153.7, 146.0, 134.2, 133.0, 119.4, 104.7, 67.6, 59.3, 36.4. +ESMS Found 269.1263 (M+H)+ C11H17N4O4 requires 269.1250.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853224B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-5a5b09708f964867aed88bd68a963f7e |
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| Source note | uspto-grants-2014_10 |
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