Dichloromethane → HCID 178435302, compound

HRID 202914Notes

Reaction equation

HRID 202914 reaction equation
[CH3:91][CH2:92][O:93][C:94]([CH3:95])=[O:96].[CH:79]([N:80]([CH2:81][CH3:82])[CH:83]([CH3:84])[CH3:85])([CH3:86])[CH3:87].[Cl:88][CH2:89][Cl:90].[NH2:40][C:41]1([C:46](=[O:47])[NH:48][S:49](=[O:50])(=[O:51])[CH:52]2[CH2:53][CH2:54]2)[CH:42]([CH:44]=[CH2:45])[CH2:43]1.[P-:55]([F:56])([F:57])([F:58])([F:59])([F:60])[F:61].[c:1]1(-[c:34]2[cH:35][cH:36][cH:37][cH:38][cH:39]2)[cH:2][cH:3][c:4]([C:7]2([S:30][CH:31]([CH3:32])[CH3:33])[CH2:8][CH:9]([C:27](=[O:28])[OH:29])[N:10]([C:12]([CH:13]([C:14]([CH3:15])([CH3:16])[CH3:17])[NH:18][C:19](=[O:20])[O:21][C:22]([CH3:23])([CH3:24])[CH3:25])=[O:26])[CH2:11]2)[cH:5][cH:6]1.[n:62]1([O:63][C:64]([N:65]([CH3:66])[CH3:67])=[N+:68]([CH3:69])[CH3:70])[c:71]2[n:72][cH:73][cH:74][cH:75][c:76]2[n:77][n:78]1>>[c:1]1(-[c:34]2[cH:35][cH:36][cH:37][cH:38][cH:39]2)[cH:2][cH:3][c:4]([C:7]2([S:30][CH:31]([CH3:32])[CH3:33])[CH2:8][CH:9]([C:27](=[O:29])[NH:40][C:41]3([C:46](=[O:47])[NH:48][S:49](=[O:50])(=[O:51])[CH:52]4[CH2:53][CH2:54]4)[CH:42]([CH:44]=[CH2:45])[CH2:43]3)[N:10]([C:12]([CH:13]([C:14]([CH3:15])([CH3:16])[CH3:17])[NH:18][C:19](=[O:20])[O:21][C:22]([CH3:23])([CH3:24])[CH3:25])=[O:26])[CH2:11]2)[cH:5][cH:6]1

Participants

8

Reactant 7

HCID 6344DichloromethaneHCID 8857Ethyl AcetateHCID 9886HexafluorophosphateHCID 81531DiisopropylethylamineHCID 4641409(Dimethylamino)-N,N-dimethyl(3H-(1,2,3)triazolo(4,5-b)pyridin-3-yloxy)methaniminiumHCID 222502241-Amino-N-(cyclopropylsulfonyl)-2-vinylcyclopropane-1-carboxamideHCID 1784607031-[3,3-dimethyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoyl]-4-(4-phenylphenyl)-4-propan-2-ylsulfanylpyrrolidine-2-carboxylic acid

Product 1

HCID 178435302HCID 178435302, compound

Sources & evidence

ORD record
ord-8c01dab292934580af2278ca7a9cbc8e
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)

Reaction notes

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