HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 639311Generated: October 27, 2026
Potassium Hydroxide → 6-Cyclopropylmethoxy-5-piperidin-1-yl-pyrazine-2-carboxylic acid
https://huagongshe.com/reaction/639311
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Cyclopropanemethanol | HCID 75644 | — |
| Reactant | 6-Bromo-5-piperidin-1-yl-pyrazine-2-carboxylic acid methyl ester | HCID 86619522 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Cyclopropylmethoxy-5-piperidin-1-yl-pyrazine-2-carboxylic acid | HCID 68567998 | 10% |
Reaction Steps
A mixture of 0.12 g (0.4 mmol) 6-bromo-5-piperidin-1-yl-pyrazine-2-carboxylic acid methyl ester, 0.029 g (0.4 mmol) cyclopropyl methanol and 0.018 g (0.41 mmol) NaH (55% suspension in oil) in 2 mL DMF was shaken for an extended period of time. Afterwards, 0.1 mL KOH (5N aq.) was added and the mixture was heated to 45° C. for 1 h. After addition of formic acid the mixture was subjected to purification by preparative HPLC on reversed phase eluting with a gradient formed from acetonitrile, water and formic acid. The combined product fractions were evaporated to yield 11 mg (10%) of the title compound. m/z (ES+): 278.1 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07691863B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-4d9434024e06406c94eb29c10e1a0e69 |
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| Source note | uspto-grants-2010_04 |
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