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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411047Generated: October 30, 2026

4,4-Difluoropiperidine → HCID 86656969, compound

https://huagongshe.com/reaction/411047

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,4-DifluoropiperidineHCID 2758352—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86656968HCID 86656968—
SolventDichloromethaneHCID 6344—
ProductHCID 86656969HCID 8665696944.5%

Reaction Steps

2-(6-Chloro-benzothiazol-2-ylamino)-1-methyl-1H-benzoimidazole-5-carboxylic acid [2 (4,4-difluoro-piperidin-1-yl)-ethyl]-amide (45 mg) was prepared by following General Procedure P starting from 2-(6-chloro-benzothiazol-2-ylamino)-1-methyl-1H-benzoimidazole-5-carboxylic acid (2-oxo-ethyl)-amide (80 mg), 4,4-difluoro-piperidine (36 mg), and Na(OAc)3BH (65 mg) in DCM (2 mL). LC/MS: m/z 504.5. 1H NMR (DMSO-d6, 400 MHz): δ 8.97-8.88 (m, 1H), 8.14-8.12 (m, 1H), 7.97-7.96 (m, 1H), 7.88-7.80 (m, 1H), 7.56-7.52 (m, 2H), 7.43-7.40 (m, 1H), 4.08-4.05 (m, 1H), 3.74-3.69 (m, 7H), 3.57-3.47 (m, 1H), 3.46-3.17 (m, 3H), 2.46-2.43 (m, 3H), —NH proton signal was not observed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759535B2
Source datasetuspto-grants-2014_06
ORD IDord-ed35ba5bf79543d39c78b7c4f035b749
Source noteuspto-grants-2014_06