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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111925Generated: October 28, 2026

Dichloromethane → HCID 68577174, compound

https://huagongshe.com/reaction/2111925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1,3-Thiazole-2-carbaldehydeHCID 2734903—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 43652145HCID 43652145—
SolventEthyl AcetateHCID 8857—
ProductHCID 68577174HCID 6857717476.6%

Reaction Steps

Sodium triacetoxyborohydride (0:30 g, 1.42 mmol) is added to a stirred solution of 4-(3-methyl-butylamino)-piperidine-1-carboxylic acid tert-butyl ester (0.19 g, 0.71 mmol), 2-thiazolecarboxaldehyde (0.12 ml, 1.42 mmol), and dichloromethane (3.5 ml). The reaction is stirred overnight at room temperature under nitrogen. The reaction is diluted with ethyl acetate, washed with aqueous saturated NaHCO3, dried over Na2SO4, filtered, and concentrated. Water is added to the residue, and the solution loaded onto a SCX-2 (10 g) column and washed with water (20 ml) and methanol (20 ml). The product is then eluted with 2M ammonia in methanol (30 ml). The filtrate is concentrated and the crude material purified on silica gel eluting with 0-50% ethyl acetate/hexanes to yield (0.20 g) of 4-{(3-methyl-butyl)-[(thiazol-2-yl)-methyl]-amino}-piperidine-1-carboxylic acid tert-butyl ester: mass spectrum (ion spray): m/z=368 (M+1); 1H NMR (CDCl3): δ=7.67 (1H, d), 7.23 (1H, d), 4.17 (2H, brs), 3.93 (2H, s), 2.72-2.54 (5H, m), 1.78 (2H, brd), 1.7-1.57 (2H, m), 1.45-1.41 (10H, m), 1.40-1.32 (2H, m), 0.87 (6H, d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521462B2
Source datasetuspto-grants-2009_04
ORD IDord-2364e6dd9aff4992a6dd5bb2aaf0d10a
Source noteuspto-grants-2009_04