Tetrahydrofuran → HCID 66851894, compound

HRID 1238223Notes

Reaction equation

HRID 1238223 reaction equation
[C:1]([CH3:2])([CH3:3])([CH3:4])[c:5]1[cH:6][n:7]([CH2:11][C:12]2([OH:15])[CH2:13][CH2:14]2)[c:8](=[NH:10])[s:9]1.[CH2:39]1[O:40][CH2:41][CH2:42][CH2:43]1.[CH3:32][CH2:33][N:34]([CH2:35][CH3:36])[CH2:37][CH3:38].[Cl:16][c:17]1[cH:18][cH:19][c:20]([O:26][CH3:27])[c:21]([C:22](=[O:23])[OH:24])[cH:25]1.[S:28]([Cl:29])([Cl:30])=[O:31]>>[C:1]([CH3:2])([CH3:3])([CH3:4])[c:5]1[cH:6][n:7]([CH2:11][C:12]2([OH:15])[CH2:13][CH2:14]2)[c:8](=[N:10][C:22]([c:21]2[c:20]([O:26][CH3:27])[cH:19][cH:18][c:17]([Cl:16])[cH:25]2)=[O:23])[s:9]1

Participants

6

Reactant 5

HCID 8028TetrahydrofuranHCID 8471TriethylamineHCID 24386Thionyl ChlorideHCID 769705-Chloro-o-anisic acidHCID 668519251-((5-tert-butyl-2-iminothiazol-3(2H)-yl)methyl)cyclopropanol

Product 1

HCID 66851894HCID 66851894, compound

Sources & evidence

ORD record
ord-e4b25df611de44b8a92fa433247cb121
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (5/10)

Reaction notes

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