HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516116Generated: October 30, 2026
Diisopropylethylamine → HCID 86654743, compound
https://huagongshe.com/reaction/516116
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (1S,2R)-Cyclohexane-1,2-diamine, N1-BOC protected | HCID 1514389 | — |
| Reactant | HCID 86654744 | HCID 86654744 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86654743 | HCID 86654743 | 55.5% |
Reaction Steps
In a 10 mL sealed cap glass vial, 4,6-dichloro-2-(2,4-dimethoxybenzyl)-7-fluoro-1,1-dimethyl-1H-pyrrolo[3,4-c]pyridin-3(2H)-one (50 mg, 0.125 mmol) and tert-butyl (1S,2R)-2-aminocyclohexylcarbamate (53.2 mg, 0.250 mmol) were dissolved in ACN (2 mL). N-ethyldiisopropylamine (0.033 mL, 0.188 mmol) was added, the cap was sealed, and the reaction mixture heated at 95° C. for 72 h. The reaction mixture was subsequently purified by preparative HPLC and basified to give the title compound as a light yellow solid (40 mg, 55%). [M+H] calc'd for C29H38ClFN4O5, 578.1; found, 577.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108970B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-cb39d8e63807456693d1477924ccb207 |
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| Source note | uspto-grants-2015_08 |
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