Dichloromethane → HCID 178473622, compound

HRID 94314Notes

Reaction equation

HRID 94314 reaction equation
[CH:39]([N:40]([CH:41]([CH3:42])[CH3:43])[CH2:44][CH3:45])([CH3:46])[CH3:47].[Cl:90][CH2:91][Cl:92].[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.[SH:63][CH:64]1[CH2:65][CH:66]([CH2:82][S:83][c:84]2[cH:85][cH:86][n:87][cH:88][cH:89]2)[N:67]([C:69](=[O:70])[O:71][CH2:72][c:73]2[cH:74][cH:75][c:76]([N+:79](=[O:80])[O-:81])[cH:77][cH:78]2)[CH2:68]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:63][CH:64]4[CH2:65][CH:66]([CH2:82][S:83][c:84]5[cH:85][cH:86][n:87][cH:88][cH:89]5)[N:67]([C:69](=[O:70])[O:71][CH2:72][c:73]5[cH:74][cH:75][c:76]([N+:79](=[O:80])[O-:81])[cH:77][cH:78]5)[CH2:68]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

6

Reactant 5

HCID 6344DichloromethaneHCID 67749Trifluoromethanesulfonic anhydrideHCID 81531DiisopropylethylamineHCID 14305046(4-Nitrophenyl)methyl 6-[1-[(4-nitrophenyl)methoxycarbonyloxy]ethyl]-3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylateHCID 178525203(4-nitrophenyl)methyl 2-(pyridin-4-ylsulfanylmethyl)-4-sulfanylpyrrolidine-1-carboxylate

Product 1

HCID 178473622HCID 178473622, compound

Sources & evidence

ORD record
ord-74566416290c4d5e892c32909025d222
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (2/10)

Reaction notes

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