HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474326Generated: October 31, 2026
3-Pyridinemethanol → HCID 58063073, compound
https://huagongshe.com/reaction/474326
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Pyridinemethanol | HCID 7510 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | HCID 86661440 | HCID 86661440 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58063073 | HCID 58063073 | 68% |
Reaction Steps
To a degassed solution of 3-pyridylcarbinol (17.6 mg, 0.16 mM, 1.5 equiv) in 0.8 mL of DMF was added a one molar solution of lithium hexamethyldisilazide (215 uL, 0.22 mM, 2.0 equiv). This mixture was stirred for 10 minutes then added dropwise to a stirred solution of 5-chloro-N-isopropylpyrazolo[1,5-c]pyrimidine-3-carboxamide (25.7 mg, 0.11 mM, 1.0 equiv) in one mL of DMF. The reaction mixture was purified using reversed phase HPLC (5 to 30% acetonitrile/water, 0.1% formic acid) and the product lyophilized to give 22.7 mg (68%) of N-isopropyl-5-(pyridin-3-ylmethoxy)pyrazolo[1,5-a]pyrimidine-3-carboxamide. LCMS (ESI) m+H=312.2, 1H NMR (400 MHz, DMSO-d6) δ: 9.09 (d, 1H), 8.76 (d, 1H), 8.59 (dd, 1H), 8.38 (s, 1H), 7.95 (d, 1H), 7.45 (dd 2H), 6.81 (d, 1H), 5.61 (s, 1H), 4.08 (m, 1H), 1.19 (d, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637526B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-6cf154564cbc4fb888df61b4e1a21b47 |
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| Source note | uspto-grants-2014_01 |
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