Dichloromethane → HCID 178473621, compound

HRID 1565263Notes

Reaction equation

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

Participants

Reactant 5

HCID 6344Dichloromethane

HCID 67749Trifluoromethanesulfonic anhydride

HCID 81531Diisopropylethylamine

HCID 14305046(4-Nitrophenyl)methyl 6-[1-[(4-nitrophenyl)methoxycarbonyloxy]ethyl]-3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate

HCID 19884022HCID 19884022, compound

Product 1

HCID 178473621HCID 178473621, compound

Sources & evidence

ORD record: ord-7d09b7be025944dc90ee4bbacf97d71b
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (1/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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