Hydrochloric Acid → HCID 178483243, compound

HRID 86816Notes

Reaction equation

HRID 86816 reaction equation
[C:13]([CH3:14])([CH3:15])([CH3:16])[O:17][C:18](=[O:19])[NH:20][C:21]([CH2:22][CH:23]=[CH:24][C:25](=[O:26])[OH:27])([CH3:28])[CH3:29].[CH2:40]([c:41]1[cH:42][cH:43][cH:44][cH:45][cH:46]1)[CH:47]([C:48](=[O:49])[N:50]1[CH:51]([CH2:55][N:56]([CH3:57])[CH3:58])[CH2:52][CH2:53][CH2:54]1)[N:59]([C:60]([CH:61]([CH2:62][c:63]1[cH:64][c:65]2[cH:66][cH:67][cH:68][cH:69][c:70]2[cH:71][cH:72]1)[NH:73][CH3:74])=[O:75])[CH3:76].[CH2:85]([N:86]([CH:87]([CH3:88])[CH3:89])[CH:90]([CH3:91])[CH3:92])[CH3:93].[CH3:2][N:3]([CH3:4])[CH2:5][CH2:6][CH2:7][N:8]=[C:9]=[N:10][CH2:11][CH3:12].[CH3:80][N:81]([CH3:82])[CH:83]=[O:84].[CH3:94][CH2:95][O:96][C:97](=[O:98])[CH3:99].[Cl:77][CH2:78][Cl:79].[ClH:1].[OH:30][n:31]1[c:32]2[n:33][cH:34][cH:35][cH:36][c:37]2[n:38][n:39]1>>[C:13]([CH3:14])([CH3:15])([CH3:16])[O:17][C:18](=[O:19])[NH:20][C:21]([CH2:22][CH:23]=[CH:24][C:25](=[O:27])[N:73]([CH:61]([C:60]([N:59]([CH:47]([CH2:40][c:41]1[cH:42][cH:43][cH:44][cH:45][cH:46]1)[C:48](=[O:49])[N:50]1[CH:51]([CH2:55][N:56]([CH3:57])[CH3:58])[CH2:52][CH2:53][CH2:54]1)[CH3:76])=[O:75])[CH2:62][c:63]1[cH:64][c:65]2[cH:66][cH:67][cH:68][cH:69][c:70]2[cH:71][cH:72]1)[CH3:74])([CH3:28])[CH3:29]

Participants

10

Reactant 9

HCID 313Hydrochloric AcidHCID 6228DimethylformamideHCID 6344DichloromethaneHCID 8857Ethyl AcetateHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 81531DiisopropylethylamineHCID 181649HOAtHCID 541269175-Methyl-5-[(2-methylpropan-2-yl)oxycarbonylamino]hex-2-enoic acidHCID 178483148HCID 178483148, compound

Product 1

HCID 178483243HCID 178483243, compound

Sources & evidence

ORD record
ord-3e54f321f1f540039e94ba1071602c76
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (2/10)

Reaction notes

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