HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668798Generated: October 31, 2026
Methyl chloroformate → HCID 11508604, compound
https://huagongshe.com/reaction/1668798
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 11471935 | HCID 11471935 | — |
| Catalyst | Sodium Sulfate | HCID 24436 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 11508604 | HCID 11508604 | 72% |
Reaction Steps
To a solution of (6-amino-2-methyl-quinazolin-4-yl)-(4-methoxy-phenyl)-methylamine (150 mg, 0.51 mmol) in 5 ml of THF was added potassium carbonate (160 mg, 1.16 mmol), 2 mg of sodium sulfate. The reaction mixture was cooled to 0° C., and methyl chloroformate (0.4 ml, 5 mmol) was added. The reaction mixture was stirred at 0° C. for 10-15 min, then diluted with EtOAc (20 ml), washed with water, brine, dried over Na2SO4, filtered and concentrated by vacuum. The crude product was purified by chromatography on silica gel with acetate, hexane (1:3 to 1:1) as eluent, yielding 129 mg of title compound (72%) as yellow solids. 1H NMR (CDCl3): 7.70 (s, 2H), 7.12-7.07 (m, 2H), 6.94-6.89 (m, 3H), 6.32 (brs, 1H), 3.84 (s, 3H), 3.70 (s, 3H), 3.57 (s, 3H), 2.70 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989462B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-ee00946a4d494bc3bb232704161a77c4 |
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| Source note | uspto-grants-2011_08 |
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