HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264508Generated: October 30, 2026
Methanesulfonyl chloride → HCID 86615300, compound
https://huagongshe.com/reaction/2264508
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 68779108 | HCID 68779108 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86615300 | HCID 86615300 | 93.4% |
Reaction Steps
To a stirred solution of 4-(5-hydroxy-pyrimidin-2-ylamino)-piperidine-1-carboxylic acid tert-butyl ester (0.74 g, 2.5 mmol, 1.0 equiv) in dichloromethane (20 mL) were added N-ethyl diisopropylamine (1.09 mL, 0.82 g, 6.3 mmol, 2.5 equiv), followed by methanesulfonyl chloride (0.24 mL, 0.35 g, 3.0 mmol, 1.2 equiv). After stirring for 4 h, the reaction mixture was poured into ice water and extracted twice with dichloromethane. The combined organic layers were washed with water, then dried over MgSO4, filtered and concentrated by evaporation under reduced pressure. The crude product was purified by column chromatography on silica eluting with a gradient of dichloromethane/methanol to give 0.87 g (93%) of the title compound as colorless foam. MS (ISP): 373.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07855194B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-aea8d9d930a74a93b86f89c2fd9f31da |
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| Source note | uspto-grants-2010_12 |
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