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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723311Generated: October 29, 2026

Formaldehyde → HCID 10450603, compound

https://huagongshe.com/reaction/723311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 10065666HCID 10065666—
SolventDichloromethaneHCID 6344—
ProductHCID 10450603HCID 10450603—

Reaction Steps

To a solution of 4-Benzyl-6-methyl-8-piperazin-1-yl-4H-benzo[1,4]oxazin-3-one (140 mg, 0.42 mmol) in CH2Cl2 (5 ml) from Example 1 was added formaldehyde (37 wt % solution in water, 50 μl, 0.67 mmol) and NaBH(OAc)3. The solution was stirred with a magnetic stirrer at room temperature for 2 hours, and then partitioned between CH2Cl2 (20 ml) and saturated NaHCO3 solution (20 ml). The aqueous layer was extracted with CH2Cl2 (2×20 ml). After drying over MgSO4, the organic fraction was concentrated in vacuo to give 4-Benzyl-6-methyl-8-(4-methyl-piperazin-1-yl)-4H-benzo[1,4]oxazin-3-one as yellow solid. (140 mg, 95%) MS: (M+H)+352.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141562B2
Source datasetuspto-grants-2006_11
ORD IDord-156c23fa6e284d8ca607c6e30cdc476a
Source noteuspto-grants-2006_11