HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907317Generated: October 31, 2026
Dichloromethane → HCID 131729162, compound
https://huagongshe.com/reaction/907317
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | N-Cyclopropyl-3-(2-(cyclopropylmethyl)-4-formyl-1-oxo-1,2-dihydroisoquinolin-6-yl)-5-fluoro-4-methylbenzamide | HCID 57551841 | — |
| Product | HCID 131729162 | HCID 131729162 | — |
Reaction Steps
To a solution of the product of Example 75 step i) (400 mg) in dichloromethane (20 mL) was added piperazine-1-carboxylic acid, tert-butyl ester (534 mg) and the mixture stirred at room temperature for 10 minutes before the addition of sodium triacetoxyborohydride (608 mg). After stirring at room temperature for a further 24 hours the reaction mixture was diluted with dichloromethane and washed with water. The organic phase was then evaporated to dryness and the residue treated with 4M HCl in 1,4-dioxane (10 mL) with methanol being added to aid dissolution. The reaction was stirred at room temperature for 1 hour and then concentrated to dryness. The residue was stirred in methanol and the resulting precipitate collected by filtration, washing with methanol to give the title compound as a solid (190 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08012979B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-43033afe879d47b3bdb691d453bf7046 |
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| Source note | uspto-grants-2011_09 |
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