4-(Dimethylamino)benzoic acid → HCID 22507712, compound

HRID 985835Notes

Reaction equation

HRID 985835 reaction equation
[CH3:1][N:2]([CH3:12])[C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=O)=[CH:5][CH:4]=1.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C(N(C(C)C)C(C)C)C.[O:46]1[CH2:51][CH2:50][O:49][CH2:48][CH:47]1[C:52]1[C:60]2[S:59][C:58]([NH2:61])=[N:57][C:56]=2[C:55]([O:62][CH3:63])=[CH:54][CH:53]=1>C1COCC1.C(Cl)(Cl)Cl>[CH3:12][N:2]([CH3:1])[C:3]1[CH:4]=[CH:5][C:6]([C:7]([NH:61][C:58]2[S:59][C:60]3[C:52]([CH:47]4[CH2:48][O:49][CH2:50][CH2:51][O:46]4)=[CH:53][CH:54]=[C:55]([O:62][CH3:63])[C:56]=3[N:57]=2)=[O:9])=[CH:10][CH:11]=1

Participants

7

Procedure

From 4-dimethylaminobenzoic acid, HATU and N-ethyldiisopropylamine in THF, then treatment with (+)-7-[1,4]dioxan-2-yl-4-methoxy-benzothiazol-2-ylamine. [α]D20=+22.6° (c=0.45, CHCl3), ES-MS m/e (%): 414 (M+H+, 100).

Sources & evidence

ORD record
ord-c3d4cc3395dc422cb762882d87feeed6
Source dataset
uspto-grants-2005_03
Patent number
US06872833B2

Reaction notes

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