Triethylamine → Methyl 3-[2-[2-(4-fluorophenyl)ethoxy]ethylaminosulphonyl]propanoate

HRID 1601731Notes

Reaction equation

HRID 1601731 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][O:10][CH2:11][CH2:12][NH2:13])=[CH:4][CH:3]=1.C(N(CC)CC)C.Cl[S:22]([CH2:25][CH2:26][C:27]([O:29][CH3:30])=[O:28])(=[O:24])=[O:23]>C(OCC)C>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][CH2:9][O:10][CH2:11][CH2:12][NH:13][S:22]([CH2:25][CH2:26][C:27]([O:29][CH3:30])=[O:28])(=[O:24])=[O:23])=[CH:6][CH:7]=1

Participants

5

Procedure

The subtitle compound (8.32 g) was prepared according to the method of Example 3d) using 2-[2-(4-fluorophenyl)ethoxy]ethanamine (5.36 g), triethylamine (4.6 ml) and methyl 3-(chlorosulphonyl)propanoate (5.6 g) in diethyl ether (150 ml).

Sources & evidence

ORD record
ord-22c1fdeb7a624b4fa55cddf64d13e276
Source dataset
uspto-grants-1999_11
Patent number
US05977384

Reaction notes

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