HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527038Generated: November 1, 2026
Dichloromethane → HCID 68007768, compound
https://huagongshe.com/reaction/527038
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Isocyanatocarbonyl chloride | HCID 119708 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 86667438 | HCID 86667438 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68007768 | HCID 68007768 | — |
Reaction Steps
To a solution of 2-(5-chloro-1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoro-N-((1S,3R)-3-(hydroxyamino)cyclohexyl)pyrimidin-4-amine, 55b, (0.072 g, 0.136 mmol) in THF (2 mL) at 0° C. was added N-(oxomethylene)carbamoyl chloride (0.014 mL, 0.176 mmol). A white solid formed immediately. The slurry was shaken and sonicated to make an even suspension/slurry. Then, —CH2Cl2 (1 mL)) was added to help solvate the slurry. After 135 min, the mixture was treated with NaOMe (2 mL, 25% w/v). After 2 min, the mixture was quenched with saturated NH4Cl and acidified with 1M HCl. The mixture was extracted with EtOAc (3×) and the combined organic layers were dried over Na2SO4, filtered and concentrated in vacuo. Preparative HPLC provided the desired product (25 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09345708B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-62783e8ff6f2499390afb8b2b950341f |
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| Source note | uspto-grants-2016_05 |
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