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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063576Generated: October 30, 2026

Sodium triacetoxyborohydride → 4-(8-{4-[2-(4-Hydroxy-piperidin-1-yl)-thiazol-4-ylmethyl]-[1,4]diazepan-1-yl}-6-methyl-quinolin-7-yloxy)-butyric acid methyl ester

https://huagongshe.com/reaction/2063576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-(4-Hydroxy-piperidin-1-yl)-thiazole-4-carbaldehydeHCID 59366161—
Reactant4-(8-[1,4]Diazepan-1-yl-6-methyl-quinolin-7-yloxy)-butyric acid methyl esterHCID 59366207—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
Product4-(8-{4-[2-(4-Hydroxy-piperidin-1-yl)-thiazol-4-ylmethyl]-[1,4]diazepan-1-yl}-6-methyl-quinolin-7-yloxy)-butyric acid methyl esterHCID 59366168—

Reaction Steps

The product from step 2 (3.63 mmol) was dissolved in 1,2-dichloroethane (7.26 mL), and 2-(4-Hydroxy-piperidin-1-yl)-thiazole-4-carbaldehyde (771 mg, 3.63 mmol) was then added. This solution was stirred for 1 h, then NaBH(OAc)3 (1.54 g, 7.26 mmol) was added. The solution was stirred for 2 h, then diluted with CH2Cl2. The solution was washed with sat. aq. NaHCO3, then brine. The organic was dried over MgSO4, filtered, and concentrated to give the crude product. This was carried on without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288373B2
Source datasetuspto-grants-2012_10
ORD IDord-6b85442d45754938a379b84ca4415ac0
Source noteuspto-grants-2012_10