HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17837Generated: October 27, 2026
Sodium borohydride → 6,7-dichloro-4-cyclopropyl-3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide
https://huagongshe.com/reaction/17837
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6,7-dichloro-4-cyclopropyl-4H-1,2,4-benzothiadiazine 1,1-dioxide | HCID 67530650 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 6,7-dichloro-4-cyclopropyl-3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide | HCID 44610556 | — |
Reaction Steps
Finely ground NaBH4 (1 g) is added to a solution of 6,7-dichloro-4-cyclopropyl-4H-1,2,4-benzothiadiazine 1,1-dioxide from the Step above (1.9 g) in isopropanol (50 mL) and then heated at 50-55° C. for 5-10 minutes. The solvent is removed by evaporation under reduced pressure. The residue is taken up in water (50 mL) and brought to acid pH by adding 6N HCl. The title product is extracted with dichloromethane (3×30 mL). The organic phase is dried over MgSO4 and filtered. The filtrate is evaporated to dryness and the residue obtained is recrystallised from methanol/water 1/1 (60 mL).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741320B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-a9ab08942b9a49718b6566737d411164 |
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| Source note | uspto-grants-2010_06 |
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