Trimellitic anhydride → HCID 21884392, compound

HRID 722550Notes

Reaction equation

[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([NH:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29])=[C:6]([C:8]2[O:9][C:10]3[CH:16]=[CH:15][C:14]([C:17]4[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=4)=[CH:13][C:11]=3[N:12]=2)[CH:7]=1.[CH:30]1[C:35]([C:36]([OH:38])=[O:37])=[CH:34][C:33]2[C:39]([O:41][C:42](=O)[C:32]=2[CH:31]=1)=[O:40]>>[CH2:24]([NH:23][C:5]1[CH:4]=[CH:3][C:2]([N:1]2[C:39](=[O:40])[C:33]3[C:32](=[CH:31][CH:30]=[C:35]([C:36]([OH:38])=[O:37])[CH:34]=3)[C:42]2=[O:41])=[CH:7][C:6]=1[C:8]1[O:9][C:10]2[CH:16]=[CH:15][C:14]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[CH:13][C:11]=2[N:12]=1)[CH2:25][CH2:26][CH2:27][CH2:28][CH3:29]

Participants

Reactant 2

HCID 11089Trimellitic anhydride

HCID 21884508HCID 21884508, compound

Product 1

HCID 21884392HCID 21884392, compound

Procedure

Prepared by the method of Example 1b), from 2-(5-amino-2-hexylaminophenyl)-5-phenylbenzoxazole (237 mg, 0.61 mmol) and 1,2,4-benzenetricarboxylic anhydride (117 mg, 0.61 mmol) the title compound was obtained (129 mg, 38%). 1H NMR (DMSO) δ 8.46(m, 2H), 8.30(m, 1H), 8.08(m, 2H), 7.80(m, 4H), 7.49(m, 3H), 7.40(m, 1H), 7.02(m, 1H), 3.40(m, 2H), 1.75(m, 2H), 1.41(m, 6H), 0.91(m, 3H). MS 560 m/z (M+H)+.

Sources & evidence

ORD record: ord-f7455370033349eb85f00002ee92c8f6
Source dataset: uspto-grants-2006_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07138425B2

Reaction notes

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