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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627796Generated: October 30, 2026

Sodium borohydride → HCID 71143632, compound

https://huagongshe.com/reaction/627796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 71143564HCID 71143564—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 71143632HCID 71143632—

Reaction Steps

2-[2-(4-isopropylsulfonylphenyl)-5-trityl-pyrrolo[2,3-b]pyrazin-7-yl]-3-oxo-isoindoline-4-carbonitrile (150 mg, 0.2143 mmol) dissolved in a mixture of DCM (10 mL) and MeOH (5 mL) under N2. CoCl2 (55.65 mg, 0.4286 mmol) added then the reaction mixture cooled in an ice bath. NaBH4 (81 mg, 2.143 mmol) added in one portion. Ice bath removed and mixture stirred for 3 h then cooled in an ice bath and water (˜5 mL) added. Mixture diluted with DCM (˜20 mL) and stirred vigorously for 20 mins. Layers separated and aqueous extracted with DCM. Aqueous phase basified by addition of sat NaHCO3 solution and extracted with DCM (×2). Combined organics dried and concentrated to a black foam. This material deprotected using Method E Step 2 to give the title compound after purification by hplc; 1H NMR (400 MHz, DMSO) δ 1.21 (6H, d), 3.50 (1H, sep), 4.17 (2H, s), 5.50 (2H, s), 7.51-7.53 (1H, m), 7.62-7.65 (3H, m), 8.00 (2H, d), 8.51-8.54 (3H, m), m 9.09 (1H, s) ppm; MS (ES+) 462.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309250B2
Source datasetuspto-grants-2016_04
ORD IDord-75611d7ac13842d1947eef471e330661
Source noteuspto-grants-2016_04