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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393231Generated: November 1, 2026

Sodium borohydride → HCID 16045398, compound

https://huagongshe.com/reaction/1393231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 16045318HCID 16045318—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 16045398HCID 1604539877.7%

Reaction Steps

To a solution of 12-(4-chloro-benzenesulfonyl)-4,5,12-triaza-tricyclo[6.3.1.02,6]dodeca-2(6),3-dien-7-one (58 mg, 0.16 mmol) in 2:1 MeOH/THF (3 mL) was added NaBH4 (12 mg, 0.33 mmol) in portions. After sixteen hours the reaction was quenched with half saturated KHSO4 and then diluted with EtOAc and water. The separated organic phase was washed with water (10 mL), brine (10 mL), dried over MgSO4 filtered and concentrated to yield 12-(4-chloro-benzenesulfonyl)-4,5,12-triaza-tricyclo[6.3.1.02,6]dodeca-2(6),3-dien-7-ol (44 mg, 76%) as a white fluffy solid. MS (ES) m/e 354.0. (M+H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07345056B2
Source datasetuspto-grants-2008_03
ORD IDord-ebb60900584f4e47ba39407adc4e2e05
Source noteuspto-grants-2008_03