Hydrochloric Acid → HCID 178522532, compound

HRID 110871Notes

Reaction equation

HRID 110871 reaction equation
[C:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)([c:8]1[cH:9][cH:10][cH:11][cH:12][cH:13]1)([c:14]1[cH:15][cH:16][cH:17][cH:18][cH:19]1)[n:20]1[cH:21][n:22][c:23]([CH2:25][N:26]2[C:27](=[O:45])[CH:28]([NH2:44])[N:29]=[C:30]([c:37]3[c:38]([F:43])[cH:39][cH:40][cH:41][cH:42]3)[c:31]3[c:32]2[cH:33][cH:34][cH:35][cH:36]3)[cH:24]1.[C:80](=[O:81])([OH:82])[O-:83].[CH2:69]([N:70]=[C:71]=[N:72][CH2:73][CH2:74][CH2:75][N:76]([CH3:77])[CH3:78])[CH3:79].[CH3:85][N:86]([CH3:87])[CH:88]=[O:89].[CH3:91][CH2:92][O:93][C:94](=[O:95])[CH3:96].[CH3:97][CH2:98][N:99]([CH2:100][CH3:101])[CH2:102][CH3:103].[ClH:68].[Na+:84].[OH2:90].[OH:58][n:59]1[c:60]2[cH:61][cH:62][cH:63][cH:64][c:65]2[n:66][n:67]1.[nH:46]1[c:47]([C:55](=[O:56])[OH:57])[cH:48][c:49]2[cH:50][cH:51][cH:52][cH:53][c:54]12>>[C:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)([c:8]1[cH:9][cH:10][cH:11][cH:12][cH:13]1)([c:14]1[cH:15][cH:16][cH:17][cH:18][cH:19]1)[n:20]1[cH:21][n:22][c:23]([CH2:25][N:26]2[C:27](=[O:45])[CH:28]([NH:44][C:55]([c:47]3[nH:46][c:54]4[c:49]([cH:48]3)[cH:50][cH:51][cH:52][cH:53]4)=[O:56])[N:29]=[C:30]([c:37]3[c:38]([F:43])[cH:39][cH:40][cH:41][cH:42]3)[c:31]3[c:32]2[cH:33][cH:34][cH:35][cH:36]3)[cH:24]1

Participants

12

Reactant 11

HCID 313Hydrochloric AcidHCID 769Bicarbonate IonHCID 923Sodium ionHCID 962WaterHCID 6228DimethylformamideHCID 8471TriethylamineHCID 8857Ethyl AcetateHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 72899Indole-2-carboxylic acidHCID 757711-HydroxybenzotriazoleHCID 14800342HCID 14800342, compound

Product 1

HCID 178522532HCID 178522532, compound

Sources & evidence

ORD record
ord-eac4407342164cfabb64ddcad9773f97
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (2/10)

Reaction notes

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