HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216032Generated: October 29, 2026
Triethylamine → 4-methyl-1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4yl)-piperidine-4-carboxylic acid
https://huagongshe.com/reaction/216032
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Chloro-5-methyl-7H-pyrrolo(2,3-d)pyrimidine | HCID 14809282 | — |
| Reactant | 4-Methylpiperidine-4-carboxylic acid hydrochloride | HCID 51000379 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 4-methyl-1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4yl)-piperidine-4-carboxylic acid | HCID 67036781 | 93.4% |
Reaction Steps
To a solution of 4-chloro-5-methyl-7H-pyrrolo[2,3-d]pyrimidine (0.274 g, 1.64 mmol) in isopropanol (10 mL) were added 4-methylpiperidine 4-carboxylic acid hydrochloric acid from step A (0.294 g, 1.64 mmol) and triethylamine (0.654 mL, 4.92 mmol). The reaction was heated to 180° C. for 1 hour under microwave conditions, concentrated, taken up with ice water, and neutralized to pH 3 with 6 N aq. HCl to precipitate the product. The product was collected by filtration and dried under vacuum overnight to give the title compound (0.42 g, 75%) as a gray solid. MS (ES+) [M+H]+=275.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193202B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-19066ba6d4d64d8b95399f779f2e9401 |
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| Source note | uspto-grants-2012_06 |
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