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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788035Generated: October 30, 2026

Sodium borohydride → HCID 131727373, compound

https://huagongshe.com/reaction/1788035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 131727374HCID 131727374—
SolventMethanolHCID 887—
ProductHCID 131727373HCID 13172737320.1%

Reaction Steps

0.050 g (0.12 mmol) of 2-[4-(4-chlorophenyl)piperazin-1-yl]-4-propylaminothieno[3,2-d]pyrimidin-7-ol triflate (IX) is dissolved in 1 mL of methanol and 0.020 g (0.53 mmol) of sodium borohydride is added. The reaction mixture is stirred for 16 hours at ambient temperature, then concentrated by evaporation. The residue is purified by chromatography using HPLC through an RP column (column: Microsorb, RP-C18). Corresponding fractions are combined and lyophilized. 0.013 g of product X (20%) is obtained as a powder. 1H NMR (400 MHz, DMSO): 7.26 (2H, d); 7.00 (2H, d); 5.15-5.09 (1H, m); 3.86-3.79 (4H, m), 3.63-3.55 (2H, m); 3.42-3.33 (2H, m); 3.28-3.22 (4H, m); 3.18-3.11 (1H, m); 1.63-1.52 (2H, m); 0.88 (3H, t).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511045B2
Source datasetuspto-grants-2009_03
ORD IDord-96c7d4d75bf445ef8e08b6b3aec22c59
Source noteuspto-grants-2009_03