Dodecanoyl chloride → Dodecanoyl chloride

HRID 1648729Notes

Reaction equation

[OH:1][C:2]1[C:11]([S:12](=[O:21])(=[O:20])[N:13](C(C)C)[CH:14]([CH3:16])[CH3:15])=[CH:10][C:9]([N:22]=[N:23][C:24]2[CH:29]=[CH:28][C:27]([N+:30]([O-:32])=[O:31])=[CH:26][C:25]=2[S:33]([CH3:36])(=[O:35])=[O:34])=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[C:7]2[NH:37][S:38]([C:41]1[CH:42]=[C:43]([S:47]([O-:50])(=[O:49])=[O:48])[CH:44]=[CH:45][CH:46]=1)(=[O:40])=[O:39].[Na+:51].[C:52]([Cl:65])(=[O:64])[CH2:53][CH2:54][CH2:55][CH2:56][CH2:57][CH2:58][CH2:59][CH2:60][CH2:61][CH2:62][CH3:63].C(Cl)(=O)CCCCCCCCCCCCC>>[OH:1][C:2]1[C:11]([S:12](=[O:20])(=[O:21])[NH:13][CH:14]([CH3:15])[CH3:16])=[CH:10][C:9]([N:22]=[N:23][C:24]2[CH:29]=[CH:28][C:27]([N+:30]([O-:32])=[O:31])=[CH:26][C:25]=2[S:33]([CH3:36])(=[O:35])=[O:34])=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[C:7]2[NH:37][S:38]([C:41]1[CH:42]=[C:43]([S:47]([O-:50])(=[O:49])=[O:48])[CH:44]=[CH:45][CH:46]=1)(=[O:39])=[O:40].[Na+:51].[C:52]([Cl:65])(=[O:64])[CH2:53][CH2:54][CH2:55][CH2:56][CH2:57][CH2:58][CH2:59][CH2:60][CH2:61][CH2:62][CH3:63]

Participants

Reactant 3

HCID 8166Dodecanoyl chloride

HCID 66986Myristoyl chloride

HCID 135773246HCID 135773246, compound

Product 2

HCID 8166Dodecanoyl chloride

HCID 135773233HCID 135773233, compound

Procedure

In this case, sodium 3-{N-[5-hydroxy-8-(2-methylsulfonyl-4-nitrophenylazo)-6-(N,N-diisopropylsulfamoyl)naphthyl]sulfamoyl}benzenesulfonate and lauroyl chloride or myristoyl chloride were used as the raw materials for producing Compound 35 or 36, and sodium 3-{N-[5-hydroxy-8-(2-methylsulfonyl-4-nitrophenylazo)-6-(N-isopropylsulfamoyl)naphthyl]sulfamoyl}benzenesulfonate and lauroyl chloride were used for producing Compound 41.

Sources & evidence

ORD record: ord-e8cffa3ecd9946d892b587acf266d180
Source dataset: uspto-grants-1983_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04412951

Reaction notes

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