4-Morpholinobenzoate → HCID 67112416, compound

HRID 2284257Notes

Reaction equation

[NH2:1][C:2]1[CH:10]=[CH:9][C:8]2[C:4](=[CH:5][N:6]([C:11]3[CH:16]=[CH:15][C:14]([N+:17]([O-:19])=[O:18])=[CH:13][CH:12]=3)[N:7]=2)[CH:3]=1.[O:20]1[CH2:25][CH2:24][N:23]([C:26]2[CH:34]=[CH:33][C:29]([C:30]([O-])=[O:31])=[CH:28][CH:27]=2)[CH2:22][CH2:21]1>>[O:20]1[CH2:21][CH2:22][N:23]([C:26]2[CH:27]=[CH:28][C:29]([C:30]([NH:1][C:2]3[CH:10]=[CH:9][C:8]4[C:4](=[CH:5][N:6]([C:11]5[CH:12]=[CH:13][C:14]([N+:17]([O-:19])=[O:18])=[CH:15][CH:16]=5)[N:7]=4)[CH:3]=3)=[O:31])=[CH:33][CH:34]=2)[CH2:24][CH2:25]1

Participants

Reactant 2

HCID 51582824-Morpholinobenzoate

HCID 67112514HCID 67112514, compound

Product 1

HCID 67112416HCID 67112416, compound

Procedure

Compound 540 was prepared according to the procedure described in Scheme IV from 5-amino-2-(4-nitrophenyl)indazole and 4-morpholinobenzoate. [M+H]+ calcd for C24H21N5O4: 444.16; found: 444.27.

Sources & evidence

ORD record: ord-f713aeb108e8488282abed2f8b6fbb10
Source dataset: uspto-grants-2015_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09144557B2

Reaction notes

Loading…