HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280743Generated: October 31, 2026
Isopropylamine → Ethyl 4-(Isopropylamino)-2-(methylthio)pyrimidine-5-carboxylate
https://huagongshe.com/reaction/2280743
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | 4-Chloro-2-(methylthio)pyrimidine-5-carboxylic acid ethyl ester | HCID 80008 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 4-(Isopropylamino)-2-(methylthio)pyrimidine-5-carboxylate | HCID 10491237 | 92% |
Reaction Steps
A mixture of ethyl 4-chloro-2-(methylthio)pyrimidine-5-carboxylate (10 g, 43.0 mmol), propan-2-amine (4.21 mL, 49.4 mmol) and DIEA (9.76 mL, 55.9 mmol) in ethanol (140 mL) was heated at 60° C. overnight. After cooling to room temperature, the solvent was concentrated under reduced pressure and water was added. The aqueous phase was extracted three times with ethyl acetate and the combined organic phases were dried over magnesium sulfate, filtered and evaporated to give ethyl 4-(isopropylamino)-2-(methylthio)pyrimidine-5-carboxylate (10.10 g, 39.5 mmol, 92% yield) as a colorless oil. MS (ESI) m/z 256.1 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09139534B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-0e95d47c47ca47e487020a94ad3682b3 |
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| Source note | uspto-grants-2015_09 |
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