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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388804Generated: October 29, 2026

Hydrochloric Acid → HCID 66810908, compound

https://huagongshe.com/reaction/388804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 66811036HCID 66811036—
SolventDichloromethaneHCID 6344—
ProductHCID 66810908HCID 6681090887%

Reaction Steps

To a suspension of the bis HCl salt of 2-tert-butyl-1H-benzoimidazole-4-carboxylic acid (piperidin-4-ylmethyl)amide (4.28 g, 11.06 mmol) in dichloromethane (55 mL) at room temperature was added N,N-diisopropylethylamine (1.71 g, 2.31 mL), 1-(tert-butoxycarbonyl)piperidine-4-carboxaldehyde (2.58 g, 12.17 mmol) and sodium triacetoxyborohydride (3.28 g, 15.48 mmol) sequentially. The resulting mixture was stirred at room temperature for 2 h then extracted with 1M aqueous hydrochloric acid. The combined aqueous layers were basified to pH 12 with sodium hydroxide pellets, then extracted with dichloromethane. The combined organic layers were dried over sodium sulfate, filtered and evaporated. The resulting residue was dried under high vacuum to give a light brownish foam (4.9 g, 9.6 mmol, 87%) which was used without further purification. (m/z): [M+H]+ calcd for C29H45N5O3 512.35. found: 512.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377964B2
Source datasetuspto-grants-2013_02
ORD IDord-3b4f6407fd05432caf5ef481a588c231
Source noteuspto-grants-2013_02