Sodium triacetoxyborohydride → 3-(3-Benzyloxy-cyclobutylamino)-5-(3,3-dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid methyl ester

HRID 1886994Notes

Reaction equation

HRID 1886994 reaction equation
Cl.[CH3:2][O:3][C:4]([C:6]1[S:7][C:8]([C:12]#[C:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[CH:9][C:10]=1[NH2:11])=[O:5].[CH2:18]([O:25][CH:26]1[CH2:29][C:28](=O)[CH2:27]1)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>C(Cl)Cl.C(OCC)(=O)C>[CH3:2][O:3][C:4]([C:6]1[S:7][C:8]([C:12]#[C:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[CH:9][C:10]=1[NH:11][CH:28]1[CH2:29][CH:26]([O:25][CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH2:27]1)=[O:5]

Participants

6

Reactant 3

HCID 5049666Sodium triacetoxyborohydrideHCID 149327873-(Benzyloxy)cyclobutan-1-oneHCID 1317307523-Amino-5-(3,3-dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid methyl ester, hydrochloride salt

Product 1

HCID 581139753-(3-Benzyloxy-cyclobutylamino)-5-(3,3-dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid methyl esterYield 115.7%

Reagents, catalysts & solvents 2

HCID 6344DichloromethaneSolventHCID 8857Ethyl AcetateSolvent

Procedure

A mixture of 3-amino-5-(3,3-dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid methyl ester, hydrochloride salt (750 mg, 2.74 mmol) and 3-benzyloxy-cyclobutanone (2.5 g, 14.3 mmol) in DCM (40 mL) was treated with sodium triacetoxyborohydride (3.34 g, 15.8 mmol) portionwise. The mixture was stirred at room temperature for 3 hours. The solution was diluted with ethyl acetate, washed sequentially with saturated aqueous sodium bicarbonate, water, and brine. The organic phase was dried over magnesium sulfate, filtered and concentrated. The residue was purified by silica gel chromatography (0-10% ethyl acetate:hexanes). This resulted in 1.26 g (quant. yield) of 3-(3-benzyloxy-cyclobutylamino)-5-(3,3-dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid methyl ester as a mixture of cis- and trans-isomers.

Workup

  1. washwashed sequentially with saturated aqueous sodium bicarbonate, water, and brine
  2. dry with materialThe organic phase was dried over magnesium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customThe residue was purified by silica gel chromatography (0-10% ethyl acetate:hexanes)

Sources & evidence

ORD record
ord-f0bd90a70f324580bc2d153b8edd142a
Source dataset
uspto-grants-2013_08
Patent number
US08501714B2

Reaction notes

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