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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050500Generated: November 4, 2026

Acetic Acid → Hydrochloric Acid

https://huagongshe.com/reaction/1050500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetoneHCID 180—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 118115527HCID 118115527—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHydrochloric AcidHCID 313222%
ProductHCID 118114850HCID 118114850—

Reaction Steps

To a solution of (R)-3-(3-aminopiperidin-1-yl)-5-(4-(morpholine-4-carbonyl)phenylamino)-1,2,4-triazine-6-carboxamide HCl salt (100 mg, 0.21 mmol) in 1,2-dichloroethane (10 mL) and dioxane (10 mL) was added DIEA (0.18 mL, 1.05 mmol) and then acetone (0.31 mL, 4.2 mmol). The mixture was stirred for 3 h at RT. To the mixture was added HOAc (0.12 mL, 2.1 mmol) and then NaBH(OAc)3 (223 mg, 1.05 mmol). The mixture was stirred at RT overnight and then water (2 mL) was added. The mixture was concentrated in vacuo and subjected to reverse phase preparative HPLC to afford the title compound as HCl salt (50) (17 mg). MS found for C23H32N8O3 as (M+H)+ 469.2, (M−H)− 467.3. UV: λ=268 nm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382246B2
Source datasetuspto-grants-2016_07
ORD IDord-d0d9a54a653e472faec52ca6eceeb0fb
Source noteuspto-grants-2016_07