Acetate → Methyl 1(7-chloroquinazolin-4-yl)-5-methoxy-2-methylindol-3-ylacetate

HRID 2327713Notes

Reaction equation

HRID 2327713 reaction equation
[CH3:35][C:36](=[O:37])[O-:38].[CH3:39][C:40](=[O:41])[OH:42].[Cl-:33].[ClH:44].[N:29]([O-:30])=[O:31].[NH2:1][c:2]1[cH:3][cH:4][c:5]2[c:6](-[n:12]3[c:13]([CH3:28])[c:14]([CH2:23][C:24](=[O:25])[O:26][CH3:27])[c:15]4[cH:16][c:17]([O:21][CH3:22])[cH:18][cH:19][c:20]34)[n:7][cH:8][n:9][c:10]2[cH:11]1.[Na+:32].[Na+:34].[OH2:43]>>[c:2]1([Cl:33])[cH:3][cH:4][c:5]2[c:6](-[n:12]3[c:13]([CH3:28])[c:14]([CH2:23][C:24](=[O:25])[O:26][CH3:27])[c:15]4[cH:16][c:17]([O:21][CH3:22])[cH:18][cH:19][c:20]34)[n:7][cH:8][n:9][c:10]2[cH:11]1

Participants

9

Reactant 8

HCID 175AcetateHCID 176Acetic AcidHCID 312ChlorideHCID 313Hydrochloric AcidHCID 923Sodium ion2×HCID 946NitriteHCID 962WaterHCID 21449377HCID 21449377, compound

Product 1

HCID 21449337Methyl 1(7-chloroquinazolin-4-yl)-5-methoxy-2-methylindol-3-ylacetate

Sources & evidence

ORD record
ord-608f8d74b76342558a29b9d08fb00f09
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)

Reaction notes

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