HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620106Generated: October 29, 2026
Hydrochloric Acid → HCID 178447251, compound
https://huagongshe.com/reaction/620106
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | HCID 178450671 | HCID 178450671 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178447251 | HCID 178447251 | 92.6% |
Reaction Steps
One gram of 2-pivaloylamino-4-hydroxy-6-(4-tert.butoxycarbonylphenylethynyl)pyrido[2,3-d]pyrimidine is added to 25 ml of nitromethane saturated with hydrogen chloride gas at 0° C. After stirring at 0° C., the reaction mixture is allowed to reach room temperature and stirred for an additional hour. The suspension is diluted with anhydrous ether and suction filtered. The collected solid is washed with ether, methanol, and ether again, and then dried under reduced pressure to give 0.81 g of 2-pivaloylamino-4-hydroxy-6-(4-carboxyphenylethynyl)pyrido[2,3-d]pyrimidine as a yellowish powder: m.p. >250° C.; NMR (CDCl3, 300 MHz) delta 1.25 (s, 9H), 7.72 (d, 2H, J=8.02 Hz), 7.98 (d, 2H, J=8.02 Hz), 8.52 (d, 1H, J=2.01 Hz), 9.01 (d, 1H, J=2.01 Hz); IR (KBr) 3420, 3000, 1725, 1680, 1425, 1405, 1360, 1250, 1130, 1020, and 800 cm -1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04818819 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-88f7dd9943af4d769db5aae5fa8c517f |
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| Source note | uspto-grants-1989_04 |
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