HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655903Generated: November 3, 2026
Methyl chloroformate → HCID 19789645, compound
https://huagongshe.com/reaction/1655903
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4H-Pyrido(1,2-a)pyrimidine-3-carboxylic acid, 6-methyl-4-oxo- | HCID 208416 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 19789645 | HCID 19789645 | 75.9% |
Reaction Steps
A mixture containing i6.32 g (0.08 mol) of 6-methyl-4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carboxylic acid and 12.4 ml (0.088 mol) of triethylamine in 480 ml of chloroform is cooled below -10° C. by ice-salt. A solution of 6.5 ml (0.08 mol) of methyl chloroformate in 40 ml of chloroform is dropped to the above mixture at a temperature between -12° C. and -15° C. during 15 minutes. After stirring for 5 minutes, 6.43 g (0.088 mol) of butylamine dissolved in 80 ml of chloroform are dropped to the above solution at a temperature between -10° C. and -15° C. during 50 minutes. The reaction mixture is stirred for 1 hour at the same temperature and then let to stand under cooling by ice. For working up, the mixture is washed 3 times with 150 ml of 5% sodium hydrogen carbonate solution each and then 3 times with 150 ml of water each. The organic phase is dried over anhydrous sodium sulfate and evaporated to give 14.9 g (71.8%) of the named product as yellow crystals, m.p.: 127°-130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05252572 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-7aa8135c64604838a084d06ae844b0c7 |
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| Source note | uspto-grants-1993_10 |
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