4-Morpholinobenzoate → HCID 67113320, compound

HRID 2284255Notes

Reaction equation

[NH2:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([C:11]1[CH:16]=[CH:15][C:14]([NH2:17])=[CH:13][CH:12]=1)[N:6]=[CH:5]2.[O:18]1[CH2:23][CH2:22][N:21]([C:24]2[CH:32]=[CH:31][C:27]([C:28]([O-:30])=O)=[CH:26][CH:25]=2)[CH2:20][CH2:19]1>>[O:18]1[CH2:19][CH2:20][N:21]([C:24]2[CH:25]=[CH:26][C:27]([C:28]([NH:1][C:2]3[CH:3]=[C:4]4[C:8](=[CH:9][CH:10]=3)[N:7]([C:11]3[CH:16]=[CH:15][C:14]([N:17]5[CH2:22][CH2:23][O:18][CH2:19][CH2:20]5)=[CH:13][CH:12]=3)[N:6]=[CH:5]4)=[O:30])=[CH:31][CH:32]=2)[CH2:22][CH2:23]1

Participants

Reactant 2

HCID 51582824-Morpholinobenzoate

HCID 834142075-Amino-1-(4-aminophenyl)indazole

Product 1

HCID 67113320HCID 67113320, compound

Procedure

Compound 537 was prepared according to the procedure described in Scheme IV from 5-amino-1-(4-aminophenyl)indazole and 4-morpholinobenzoate. [M+H]+ calcd for C28H29N5O3: 484.23; found: 484.11.

Sources & evidence

ORD record: ord-5bff1769f47a467098c8176cac496a78
Source dataset: uspto-grants-2015_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09144557B2

Reaction notes

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