Chloride → HCID 178503740, compound

HRID 126582Notes

Reaction equation

HRID 126582 reaction equation
[CH2:37]1[O:38][CH2:39][CH2:40][CH2:41]1.[Cl-:17].[Cl:1][c:2]1[cH:3][c:4]2[c:5]([nH:6][c:7]([CH:9]([CH2:10][CH2:11][S:12][CH3:13])[NH2:14])[n:8]2)[cH:15][cH:16]1.[O:18]1[CH2:19][C:20](=[O:36])[N:21]([c:24]2[c:25]([N+:33](=[O:34])[O-:35])[cH:26][c:27]([C:28](=[O:29])[OH:30])[cH:31][cH:32]2)[CH2:22][CH2:23]1>>[Cl:1][c:2]1[cH:3][c:4]2[c:5]([nH:6][c:7]([CH:9]([CH2:10][CH2:11][S:12][CH3:13])[NH:14][C:28]([c:27]3[cH:26][c:25]([N+:33](=[O:34])[O-:35])[c:24]([N:21]4[C:20](=[O:36])[CH2:19][O:18][CH2:23][CH2:22]4)[cH:32][cH:31]3)=[O:29])[n:8]2)[cH:15][cH:16]1

Participants

5

Reactant 4

HCID 312ChlorideHCID 8028TetrahydrofuranHCID 670483543-Nitro-4-(3-oxomorpholin-4-yl)benzoic acidHCID 178503715HCID 178503715, compound

Product 1

HCID 178503740HCID 178503740, compound

Sources & evidence

ORD record
ord-74cc7c245ce54b08979c44c8d17baba7
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (2/10)

Reaction notes

Loading…