Imidazole → HCID 86746113, compound

HRID 1561375Notes

Reaction equation

[CH2:1]([CH3:2])[CH:3]1[C:4](=[O:56])[CH2:5][CH:6]([OH:55])[CH:7]([CH3:54])[CH:8]([C:42](=[CH:43][CH:44]2[CH2:45][CH:46]([O:51][CH3:52])[CH:47]([OH:50])[CH2:48][CH2:49]2)[CH3:53])[O:9][C:10](=[O:41])[CH:11]2[CH2:12][CH2:13][CH2:14][CH2:15][N:16]2[C:17](=[O:40])[C:18](=[O:39])[C:19]2([OH:38])[CH:20]([CH3:37])[CH2:21][CH:22]([O:35][CH3:36])[CH:23]([CH:24]([O:32][CH3:33])[CH2:25][CH:26]([CH3:31])[CH2:27][C:28]([CH3:30])=[CH:29]1)[O:34]2.[CH3:80][CH2:81][CH2:82][CH2:83][CH2:84][CH3:85].[F:62][C:63]([F:64])([F:65])[S:66]([O:67][Si:68]([CH:69]([CH3:70])[CH3:71])([CH:72]([CH3:73])[CH3:74])[CH:75]([CH3:76])[CH3:77])(=[O:78])=[O:79].[nH:57]1[cH:58][cH:59][n:60][cH:61]1>>[CH2:1]([CH3:2])[CH:3]1[C:4](=[O:56])[CH2:5][CH:6]([OH:55])[CH:7]([CH3:54])[CH:8]([C:42](=[CH:43][CH:44]2[CH2:45][CH:46]([O:51][CH3:52])[CH:47]([O:50][Si:68]([CH:69]([CH3:70])[CH3:71])([CH:72]([CH3:73])[CH3:74])[CH:75]([CH3:76])[CH3:77])[CH2:48][CH2:49]2)[CH3:53])[O:9][C:10](=[O:41])[CH:11]2[CH2:12][CH2:13][CH2:14][CH2:15][N:16]2[C:17](=[O:40])[C:18](=[O:39])[C:19]2([OH:38])[CH:20]([CH3:37])[CH2:21][CH:22]([O:35][CH3:36])[CH:23]([CH:24]([O:32][CH3:33])[CH2:25][CH:26]([CH3:31])[CH2:27][C:28]([CH3:30])=[CH:29]1)[O:34]2

Participants

Reactant 4

HCID 795Imidazole

HCID 224117-Ethyl-1,14-dihydroxy-12-[1-(4-hydroxy-3-methoxycyclohexyl)prop-1-en-2-yl]-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9]octacos-18-ene-2,3,10,16-tetrone

HCID 8058Hexane

HCID 2724529Triisopropylsilyl trifluoromethanesulfonate

Product 1

HCID 86746113HCID 86746113, compound

Sources & evidence

ORD record: ord-39a1f1c4bce340b685ba86c106f3edc9
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (1/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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