HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168217Generated: October 31, 2026
Diisopropylethylamine → HCID 86710212, compound
https://huagongshe.com/reaction/2168217
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-4-Piperidylbenzamide | HCID 118120 | — |
| Reactant | HCID 86710211 | HCID 86710211 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 86710212 | HCID 86710212 | — |
Reaction Steps
4-chloro-7-({[2-(trimethylsilyl)ethyl]oxy}methyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile D43 (100 mg) and N-4-piperidinylbenzamide (86 mg, 0.42 mmol, commercially available from e.g. Fluorochem, Alfa Aesar and Apollo) were dissolved in NMP and then N,N-diisopropylethylamine was added dropwise. The reaction mixture was carried out in the microwave at 120° C. for 45 minutes. The reaction mixture was poured onto water extracted with EtOAc (2×60 ml). Organic layers were washed water (3×20 ml), brine (30 ml), dried (MgSO4), filtered and solvent removed. Crude product obtained was purified by flash chromatography on silica gel eluting with Pet Eth/EtOAc 3/1-2/1 to give the desired product D44 in 69 mg. LCMS [MH+] [email protected] min (5 min run)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045485B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-ddff8e099e714544a241e07cc5d67ab1 |
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| Source note | uspto-grants-2015_06 |
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