HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239533Generated: November 1, 2026
HCID 57989824, compound → HCID 57989626, compound
https://huagongshe.com/reaction/239533
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57989824 | HCID 57989824 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57989626 | HCID 57989626 | 73.4% |
Reaction Steps
To a suspension of N-{3-[5-(2-cyano-4-pyrimidinyl)-2-(4-morpholinyl)-1,3-thiazol-4-yl]-2-fluorophenyl}-2,5-difluorobenzenesulfonamide (2.12 g, 3.80 mmol) in dichloromethane (DCM) (38.0 ml) at −78° C. was added DI BAL-H (18.98 ml, 18.98 mmol). The yellow suspension was slowly warmed to RT and stirred 1 hr. The reaction was quenched with Rochelle's salts and stirred about 1 hr. 4N HCl was added to clear the emulsion. The HCl solution was extracted with DCM (3×). The aqueous was passed through celite and neutralize with 6N NaOH. Solid formed during neutralizing and was filtered to obtain N-{3-[5-[2-(aminomethyl)-4-pyrimidinyl]-2-(4-morpholinyl)-1,3-thiazol-4-yl]-2-fluorophenyl}-2,5-difluorobenzenesulfonamide (1.57 g, 73%). MS (ESI): 563 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642759B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-4ef235b208d84a77bf3315f69d37a1d1 |
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| Source note | uspto-grants-2014_02 |
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