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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715664Generated: October 29, 2026

Sodium borohydride → HCID 57639375, compound

https://huagongshe.com/reaction/715664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 66672661HCID 66672661—
SolventMethanolHCID 887—
ProductHCID 57639375HCID 5763937537%

Reaction Steps

Methyl 1-hydroxy-4-{2-[(methylethyl)amino]-8-[(2,4,6-trifluorophenyl)amino]purin-9-yl}cyclohexanecarboxylate (0.300 g, 0.6 mmol) was dissolved in 3 mL of dry methanol. The solution was cooled to 0° C. before addition of solid sodium borohydride (0.300 g, 7.92 mmol). After 1 h at low temperature, the reaction was warmed to rt and stirred overnight. The reaction was quenched with 5 mL of a saturated solution of ammonium chloride. The crude product was extracted with dichloromethane (four times). The product was purified by column chromatography (75% ethyl acetate in hexanes) followed by semi-preparative HPLC. The fractions were neutralized using a resin-exchange column. (0.101 g, 37% yield). M+1: 451.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187479B2
Source datasetuspto-grants-2015_11
ORD IDord-e9e8348ebedb4da49a2ebecb551b8341
Source noteuspto-grants-2015_11