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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921241Generated: October 30, 2026

Sodium borohydride → HCID 118318885, compound

https://huagongshe.com/reaction/921241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 118318883HCID 118318883—
CatalystHCID 178425456HCID 178425456—
SolventDichloromethaneHCID 6344—
ProductHCID 118318885HCID 11831888544.7%

Reaction Steps

A mixture of (S)-ethyl 2-(2-(((2-allyl-4-fluorobenzyl)oxy)methyl)-7-(4-(allyloxy)-4-methylpiperidin-1-yl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)-2-(tert-butoxy)acetate (70 mg, 0.112 mmol) and Grubbs II catalyst (95 mg, 0.112 mmol) in DCM (70 mL) was refluxed for 2 h. It was then concentrated and the residue was dissolved in MeOH (2 mL). Sodium borohydride (4.25 mg, 0.112 mmol) was added and the reaction mixture was stirred at rt for 1 h. It was then extracted with EtOAc, washed with water. The organic layer was dried over MgSO4, filtered and concentrated. The residue was purified by biotage, eluting with 20% EtOac/hexane to isolate ethyl (2S)-2-(tert-butoxy)-2-{16-fluoro-4,24-dimethyl-11,23-dioxa-1,5,7,8-tetraazapentacyclo[22.2.2.16,9.02,7.013,18]nonacosa-2,4,6(29),8,13(18),14,16-heptaen-3-yl}acetate (30 mg, 0.050 mmol, 44.7% yield) as a white solid. LCMS (M+1)=597.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273067B2
Source datasetuspto-grants-2016_03
ORD IDord-c944a06a4f8b4e0eb2b226a8457240d5
Source noteuspto-grants-2016_03