HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370679Generated: October 31, 2026
Hydrochloric Acid → Methyl 2-chloropyrimidine-5-carboxylate
https://huagongshe.com/reaction/2370679
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Methyl 2-aminopyrimidine-5-carboxylate | HCID 9793866 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Methyl 2-chloropyrimidine-5-carboxylate | HCID 12627752 | — |
Reaction Steps
Compound 207 (7 g, 0.046 mol) was added to a mixture of concentrated hydrochloric acid (15.2 mL) and CH2Cl2 (60 mL). After cooling, ZnCl2 (18.6 g, 0.138 mol) was added at 15-20° C. The mixture was stirred at 15-20° C. for 0.5 h and cooled to 5-10° C. NaNO2 (9.5 g, 0.138 mol) was added portion wise while keeping the internal temperature 5-10° C. The reaction was continued for ˜2 h. The reaction mixture was poured into ice-water (50 mL). The organic layer was separated and the aqueous phase was extracted with CH2Cl2 (30 mL*2). The combined organic extracts were concentrated to afford crude product (4.2 g). The crude compound was suspended in hexane (20 mL), heated at 60° C. for 30 minutes and filtered. The filtrate was concentrated to afford the title compound R-2-2 (3.5 g, 44.4%) as an off-white solid. LCMS (m/z): 214.1[M+42]+. 1HNMR (400 MHz, CDCl3): δ 4.00 (s, 3H), 9.15 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710219B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-5db6e8ebc99745a499c2474675402f8c |
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| Source note | uspto-grants-2014_04 |
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