Tetrahydrofuran → 2-(2-Tert-butoxycarbonylaminomethylthiophen-5-yl)carbonyl-4-chloroaniline

HRID 275854Notes

Reaction equation

HRID 275854 reaction equation
O1CCCC1.CN(OC)[C:8](=[O:17])[C:9]1[CH:14]=[C:13]([Cl:15])[CH:12]=[CH:11][C:10]=1[NH2:16].Br[C:21]1[S:22][C:23]([CH2:26][NH:27][C:28]([O:30][C:31]([CH3:34])([CH3:33])[CH3:32])=[O:29])=[CH:24][CH:25]=1.C([Li])CCC>C(OC(=O)C)C.O.CCCCCC>[C:31]([O:30][C:28]([NH:27][CH2:26][C:23]1[S:22][C:21]([C:8]([C:9]2[CH:14]=[C:13]([Cl:15])[CH:12]=[CH:11][C:10]=2[NH2:16])=[O:17])=[CH:25][CH:24]=1)=[O:29])([CH3:34])([CH3:32])[CH3:33]

Participants

8

Reactant 4

HCID 8028TetrahydrofuranHCID 2779810tert-Butyl ((5-bromothiophen-2-yl)methyl)carbamateHCID 222266052-amino-5-chloro-N-methoxy-N-methylbenzamideHCID 178418339Butyllithium

Product 1

HCID 183153332-(2-Tert-butoxycarbonylaminomethylthiophen-5-yl)carbonyl-4-chloroanilineYield 7.3%

Reagents, catalysts & solvents 3

HCID 962WaterSolventHCID 8058HexaneSolventHCID 8857Ethyl AcetateSolvent

Procedure

A tetrahydrofuran (60 ml) solution of N-methyl-N-methyloxy-2-amino-5-chlorobenzamide (4.96 g) and 2-bromo-5-tert-butoxycarbonylaminomethylthiophene (5.45 g) was cooled to −78° C. To the solution was gradually added dropwise a hexane solution of n-butyl lithium (1.6 mol/L) (47 ml). To the mixture were further added water (200 ml) and acetic acid ethyl ester (200 ml). The organic layer was washed with water and dried over anhydrous MgSO4, followed by distilling off the solvent. The residual oily compound was purified by means of a silica gel column chromatography to give 2-(2-tert-butoxycarbonylaminomethylthiophen-5-yl)carbonyl-4-chloroaniline (0.5 g) as a yellow oily product. To a methanol (8 ml) solution of this product (0.15 g) was added sodium borohydride (60 mg). The mixture was stirred for 30 minutes at room temperature, to which was added acetic acid ethyl ester (100 ml). The mixture was washed with water and dried over anhydrous MgSO4. The solvent was then distilled off. To a methanol (5 ml) solution of the residue were added 4-biphenylcarbaldehyde (100 mg) and acetic acid (40 mg). The mixture was stirred for 10 minutes at room temperature, to which was added sodium cyano borohydride (40 mg). The mixture was stirred for 30 minutes at 60° C., to which was added acetic acid ethyl ester (50 ml). The mixture was washed with water and dried over anhydrous MgSO4. The solvent was then distilled off to leave 0.2 g of a residual compound.

Workup

  1. washThe organic layer was washed with water
  2. dry with materialdried over anhydrous MgSO4
  3. distillationby distilling off the solvent
  4. customThe residual oily compound was purified by means of a silica gel column chromatography

Sources & evidence

ORD record
ord-78487c25e3104edaabeb6a076bdcb343
Source dataset
uspto-grants-2002_03
Patent number
US06352982B1

Reaction notes

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