HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366245Generated: November 3, 2026
HCID 66803505, compound → HCID 66801483, compound
https://huagongshe.com/reaction/2366245
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 66803505 | HCID 66803505 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 66801483 | HCID 66801483 | 78% |
Reaction Steps
A mixture of [2-(2-chloro-4-cyano-6-fluorophenyl)thiazolo[5,4-c]pyridin-4-yl]-carbamic acid tert-butyl ester (0.320 mmol) in HCl (4N in dioxane, 2.5 mL) was heated at 50° C. for 3 hours in a sealed vial. After cooling to room temperature, the volatiles were removed under reduced pressure and the resultant residue was partitioned between EtOAc and a saturated solution of NaHCO3. The aqueous phase was extracted with EtOAc, and the combined organic layers were washed with brine, dried (Na2SO4) and concentrated to dryness under reduced pressure to afford the title compound as a yellow solid (76 mg, 78% yield over two steps). 1H NMR (400 MHz, CDCl3): δ 8.21 (d, J=5.8 Hz, 1H), 7.69 (t, J=1.4 Hz, 1H), 7.53-7.46 (m, 2H), 4.84 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08697708B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-b08098a603394c60a7f96e540ce4ef16 |
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| Source note | uspto-grants-2014_04 |
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