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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823686Generated: October 30, 2026

Sodium triacetoxyborohydride → HCID 69314010, compound

https://huagongshe.com/reaction/1823686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl N-(3-oxopropyl)carbamateHCID 10910051—
ReactantHCID 22172631HCID 22172631—
SolventDichloromethaneHCID 6344—
ProductHCID 69314010HCID 69314010285.3%
ProductHCID 69316230HCID 69316230—

Reaction Steps

To a solution of dichloromethane (100 mL), 2-(1-amino-2-methyl-propyl)-3-benzyl-3H-pyrido[4,3-d]pyrimidin-4-one (1.92 mmol) and Na(OAc)3BH (0.814 g, 3.84 mmol), was added t-butyl-N-(3-oxopropyl)-carbamate (0.400 g, 2.30 mmol) at room temperature. The mixture was stirred at room temperature for 3 hours, after which it was diluted with dichloromethane (100 mL), washed with saturated sodium bicarbonate, water and brine, and dried over sodium sulfate. After concentration under reduced pressure, the desired product {3-[1-(3-benzyl-4-oxo-3,4-dihydro-pyrido[4,3-d]pyrimidin-2-yl)-2-methyl-propylamino]-propyl}-carbamic acid tert-butyl ester (0.850 g, 95%) was obtained in sufficiently pure form to be carried forward for use in the next step. MS (Cl) M/E: 466.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07038048B2
Source datasetuspto-grants-2006_05
ORD IDord-b8741f60d699475caba100bdab24a825
Source noteuspto-grants-2006_05