HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265901Generated: October 30, 2026
Sodium triacetoxyborohydride → HCID 178453913, compound
https://huagongshe.com/reaction/2265901
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 3-(Piperazin-1-yl)-1,2-benzoxazole | HCID 13232475 | — |
| Reactant | HCID 178453924 | HCID 178453924 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178453913 | HCID 178453913 | 64% |
Reaction Steps
A mixture of 3-piperazin-1-yl-1,2-benzisoxazole (1 g, 4.92 mmol), trans-[4-(2-oxo-ethyl)-cyclohexyl]-carbamic acid tert-butyl ester (Intermediate A) (1.3 g, 5.41 mmol), in dichloromethane (15 ml) was stirred for 15 minutes at room temperature and sodium triacetoxyborohydride (1.88 g, 8.86 mmol) was added slowly and the resulting solution was stirred for 12 hours until the TLC indicated completion of the reaction. The mixture was extracted with saturated NaHCO3-solution and two times dichloromethane. The organic layers were dried over sodium sulfate, filtrated and concentrated to dryness. The crude product was purified with column chromatography on silica gel using heptane:ethyl acetate 80:20->10:90. The product fractions were concentrated to give 1.34 g (64% yield) of a white solid. MS (m/e): 429.4 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07858630B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-a0d829c9ae874f3f95723a94f2f17bde |
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| Source note | uspto-grants-2010_12 |
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