HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175415Generated: November 2, 2026
ethyl 5-((tert-butoxycarbonyl(2-methyl-6-(((1S,2S)-2-(5-methylpyridin-2-yl)cyclopropyl)methoxy)pyrimidin-4-yl)amino)methyl)-1,3,4-thiadiazole-2-carboxylate → Methyl 5-((2-methyl-6-(((1S,2S)-2-(5-methylpyridin-2-yl)cyclopropyl)methoxy)pyrimidin-4-ylamino)methyl)-1,3,4-thiadiazole-2-carboxylate
https://huagongshe.com/reaction/2175415
Participants
| Role | Name | HCID | Charge |
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| Reactant | ethyl 5-((tert-butoxycarbonyl(2-methyl-6-(((1S,2S)-2-(5-methylpyridin-2-yl)cyclopropyl)methoxy)pyrimidin-4-yl)amino)methyl)-1,3,4-thiadiazole-2-carboxylate | HCID 86729573 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | Methyl 5-((2-methyl-6-(((1S,2S)-2-(5-methylpyridin-2-yl)cyclopropyl)methoxy)pyrimidin-4-ylamino)methyl)-1,3,4-thiadiazole-2-carboxylate | HCID 71274155 | 45.3% |
Reaction Steps
The solution of ethyl 5-((tert-butoxycarbonyl(2-methyl-6-(((1S,2S)-2-(5-methylpyridin-2-yl)cyclopropyl)methoxy)pyrimidin-4-yl)amino)methyl)-1,3,4-thiadiazole-2-carboxylate (S-7) (70 mg, 0.1294 mmol) in TFA (1 mL) was stirred at room temperature for 1 h. The solvent was removed under reduced pressure and the residue was purified by reverse phase column (Waters Sunfire Prep C18 OBD, 5-75% methanol in water with 0.1% NH3H2O modifier) to provide product as a white solid (25 mg, 21.4%). 1H NMR (400 MHz, CDCl3) δ 8.26 (s, 1H), 7.35 (dd, J=7.9, 1.7 Hz, 1H), 7.03 (d, J=7.9 Hz, 1H), 5.60 (s, 1H), 5.48 (s, 1H), 5.02 (d, J=6.3 Hz, 1H), 4.27 (ddd, J=24.1, 11.1, 7.0 Hz, 2H), 4.03 (s, 3H), 2.48 (d, J=5.8 Hz, 3H), 2.19 (s, 3H), 1.87-1.85 (m, 1H), 1.85-1.80 (m, 1H), 1.32-1.29 (m, 1H), 1.06-1.02 (m, 1H); LRMS (ESI) calculated M+H for C20H23N6O3S: 427.5. Found: 427.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09062059B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-6ee10dfa345f4475a4cea44e1c8418da |
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| Source note | uspto-grants-2015_06 |
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