HCID 14003453, compound → HCID 44433539, compound

HRID 2338033Notes

Reaction equation

HRID 2338033 reaction equation
[NH2:1][CH:2]1[C:3](=[O:23])[N:4]([CH2:15][C:16](=[O:17])[O:18][C:19]([CH3:20])([CH3:21])[CH3:22])[CH:5]([c:9]2[cH:10][cH:11][cH:12][cH:13][cH:14]2)[CH2:6][CH2:7][CH2:8]1.[O:24]=[C:25]1[NH:26][c:27]2[cH:28][cH:29][cH:30][cH:31][c:32]2[CH2:33][N:34]1[CH:35]1[CH2:36][CH2:37][N:38]([C:41](=[O:42])[Cl:43])[CH2:39][CH2:40]1>>[NH:1]([CH:2]1[C:3](=[O:23])[N:4]([CH2:15][C:16](=[O:17])[O:18][C:19]([CH3:20])([CH3:21])[CH3:22])[CH:5]([c:9]2[cH:10][cH:11][cH:12][cH:13][cH:14]2)[CH2:6][CH2:7][CH2:8]1)[C:41]([N:38]1[CH2:37][CH2:36][CH:35]([N:34]2[C:25](=[O:24])[NH:26][c:27]3[cH:28][cH:29][cH:30][cH:31][c:32]3[CH2:33]2)[CH2:40][CH2:39]1)=[O:42]

Participants

3

Reactant 2

HCID 14003453HCID 14003453, compoundHCID 183211084-(2-oxo-1,4-dihydroquinazolin-3(2H)-yl)piperidine-1-carbonyl chloride

Product 1

HCID 44433539HCID 44433539, compound

Sources & evidence

ORD record
ord-1ad96fe42b94450dbcda24478beafc7b
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)

Reaction notes

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