HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17846Generated: October 27, 2026
Sodium borohydride → 7-chloro-4-cyclopropylmethyl-3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide
https://huagongshe.com/reaction/17846
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 7-chloro-4-cyclopropylmethyl-4H-1,2,4-benzothiadiazine 1,1-dioxide | HCID 67529835 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 7-chloro-4-cyclopropylmethyl-3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide | HCID 67530111 | — |
Reaction Steps
To a solution of 7-chloro-4-cyclopropylmethyl-4H-1,2,4-benzothiadiazine 1,1-dioxide (0.7 g) in isopropanol (50 mL) there is added sodium borohydride (0.2 g) and the mixture is heated at 50° C. for 5 minutes. The reaction mixture is evaporated under reduced pressure and the residue is taken up in water (30 mL). The pH of the medium is adjusted to 5-6 by addition of 6N hydrochloric acid and the suspension is extracted three times with chloroform (30 mL). The organic phases are collected, dried over anhydrous MgSO4 and filtered. The filtrate is evaporated under reduced pressure and the residue is taken up in methanol (5 mL). Water (50 mL) is added to the methanolic solution and the precipitate which appears is collected by filtration, washed with water and dried.
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-a01501c88bd247b59f02614af6653c59 |
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| Source note | uspto-grants-2010_06 |
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