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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010543Generated: October 27, 2026

Sulfuric acid magnesium salt (1:1) → (tert-butoxy)-N-(2-{[(2-chloro(1,3-thiazol-5-yl))methyl][(4-methoxyphenyl)methyl]amino}ethyl)carboxamide

https://huagongshe.com/reaction/1010543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactant2-Chloro-1,3-thiazole-5-carbaldehydeHCID 1479765—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantTert-butyl N-(2-{[(4-methoxyphenyl)methyl]amino}ethyl)carbamateHCID 112688707—
Solvent1,2-DichloroethaneHCID 11—
Product(tert-butoxy)-N-(2-{[(2-chloro(1,3-thiazol-5-yl))methyl][(4-methoxyphenyl)methyl]amino}ethyl)carboxamideHCID 13172899668.5%

Reaction Steps

This compound was also made in a manner analogous to that set forth in Step D of Example 5, and Step A above, using 0.25 gram (0.0017 mole) of (2-chloro-1,3-thiazol-5-yl)formaldehyde, 0.47 gram (0.0017 mole) of (tert-butoxy)-N-(2-{[(4-methoxyphenyl)methyl]amino}ethyl)carboxamide, 0.54 gram (0.0025 mole) of sodium triacetoxyborohydride and 0.40 gram (0.0034 mole) of magnesium sulfate in about 10 mL of 1,2-dichloroethane. The reaction product was purified with column chromatography on silica gel. In a first chromatography, elution was accomplished using mixtures of 2% to 5% methanol in methylene chloride as eluants. In a second chromatography, elution was accomplished using a mixture of 1.5% methanol in methylene chloride as an eluant. Appropriate fractions were combined and concentrated under reduced pressure, yielding 0.48 gram of the subject compound. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977332B2
Source datasetuspto-grants-2011_07
ORD IDord-08bb04552a9841a980feb4305c89d2e8
Source noteuspto-grants-2011_07