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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946191Generated: October 31, 2026

Sodium borohydride → HCID 59605452, compound

https://huagongshe.com/reaction/1946191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 67492927HCID 67492927—
ProductHCID 59605452HCID 5960545256.2%

Reaction Steps

To a solution of 2-{3-[2-(2-ethylbenzoimidazol-1-yl)-9-methyl-6-morpholin-4-yl-9H-purin-8-yl]-3-fluoroazetidin-1-yl}-2-methylpropionic acid ethyl ester (40 mg, 0.07 mmol) in IMS (4 mL) was added NaBH4 (28 mg, 0.73 mmol) and the resulting mixture stirred at r.t for 3 h. Further NaBH4 (28 mg, 0.73 mmol) was added and the mixture stirred for a further 18 h. The reaction mixture was quenched with H2O, extracted with EtOAc and the organic phase dried (Na2SO4) and concentrated in vacuo. The resulting residue was purified by column chromatography (Si—PCC, MeOH:EtOAc, 0-10%) then dissolved in a mixture of MeCN and H2O and allowed to freeze-dry affording 850 as a white solid (20 mg, 54%). LCMS (method I): RT 2.64 min, [M+H]+ 509.4. 1H NMR (DMSO, 400 MHz): δ 8.05-8.04 (1 H, m), 7.64-7.63 (1 H, m), 7.26-7.25 (2 H, m), 4.58-4.49 (1 H, m), 4.44-4.14 (4 H, brd m), 4.08 (2 H, dd, J=18.70, 9.19 Hz), 3.81-3.74 (9 H, m), 3.28-3.26 (2 H, m), 3.19 (2 H, d, J=5.40 Hz), 1.34 (3 H, t, J=7.43 Hz), 0.91 (6 H, s)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394796B2
Source datasetuspto-grants-2013_03
ORD IDord-8d952861b3e84d87b64d37b73381ae1a
Source noteuspto-grants-2013_03