HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538115Generated: October 29, 2026
Tetrahydrofuran → HCID 44478524, compound
https://huagongshe.com/reaction/538115
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | HCID 66937073 | HCID 66937073 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 44478524 | HCID 44478524 | 90% |
Reaction Steps
To a mixture of 1-(4-chloro-1H-benzoimidazol-2-yl)-1H-pyrazole-4-carboxylic acid ethyl ester (0.180 g, 0.550 mmol), THF (3 mL), and water (1 mL), was added LiOH.H2O (95.0 mg, 2.20 mmol). The mixture was stirred 18 h at 23° C. The solvent was evaporated, water (3 mL) was added and the mixture acidified with aq. 1M HCl. The resulting white precipitate was filtered and dried to yield the titled compound (0.130 g, 90%). MS (ESI/CI): mass calcd. for C11H7ClN4O2, 262.0; m/z found, 263.0 [M+H]+. 1H NMR (400 MHz, DMSO-d6): 13.64 (s, 1H), 12.97 (s, 1H), 8.90 (s, 1H), 8.30 (s, 1H), 7.48 (d, J=7.4 Hz, 1H), 7.32 (dd, J=7.8, 1.0 Hz, 1H), 7.25 (t, J=7.9 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865713B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-9aa326a88a92432c8370092403e42f69 |
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| Source note | uspto-grants-2014_10 |
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