4-Toluenesulfonyl chloride → HCID 18979284, compound
Reaction equation
[S:1]([NH:11][C:12]1[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH:15]=[CH:14][C:13]=1[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][C:28](NO)=[O:29])([C:4]1[CH:10]=[CH:9][C:7]([CH3:8])=[CH:6][CH:5]=1)(=[O:3])=[O:2].NC1C2C(=CC=CC=2)C=CC=1CCCCCCC(OCOC)=[O:50].S(Cl)(C1C=CC(C)=CC=1)(=O)=O>>[S:1]([NH:11][C:12]1[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH:15]=[CH:14][C:13]=1[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][C:28]([OH:29])=[O:50])([C:4]1[CH:10]=[CH:9][C:7]([CH3:8])=[CH:6][CH:5]=1)(=[O:3])=[O:2]Participants
4
Procedure
7-(1-Tosylamino-2-naphthyl)heptanohydroxamic acid Using methoxymethyl 7-(1-amino-2-naphthyl)heptanoate and tosyl chloride, the procedure of Reference Example 50 was otherwise repeated to provide 7-(1-tosylamino-2-naphthyl)heptanoic acid.
Sources & evidence
- ORD record
- ord-beebb619eb154d738310c0665b5da142
- Source dataset
- uspto-grants-1998_09
- Patent number
- US05804601
Reaction notes
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