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N-[2-(2,5-dichloro-pyrimidin-4-ylamino)-cyclohexyl]-methanesulfonamide → HCID 178456191, compound

HRID 1138113
Notes
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Reaction equation

HRID 1138113 reaction equation
[CH2:1]([C:2]#[CH:3])[N:4]1[CH2:5][CH2:6][c:7]2[c:8]([cH:11][c:12]([NH2:15])[cH:13][cH:14]2)[CH2:9][CH2:10]1.[Cl:16][c:17]1[n:18][cH:19][c:20]([Cl:35])[c:21]([NH:23][CH:24]2[CH:25]([NH:30][S:31](=[O:32])(=[O:33])[CH3:34])[CH2:26][CH2:27][CH2:28][CH2:29]2)[n:22]1>>[CH2:1]([C:2]#[CH:3])[N:4]1[CH2:5][CH2:6][c:7]2[c:8]([cH:11][c:12]([NH:15][c:17]3[n:18][cH:19][c:20]([Cl:35])[c:21]([NH:23][CH:24]4[CH:25]([NH:30][S:31](=[O:32])(=[O:33])[CH3:34])[CH2:26][CH2:27][CH2:28][CH2:29]4)[n:22]3)[cH:13][cH:14]2)[CH2:9][CH2:10]1
ParticipantsSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 86633859N-[2-(2,5-dichloro-pyrimidin-4-ylamino)-cyclohexyl]-methanesulfonamideHCID 866338783-prop-2-ynyl-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ylamine

Product 1

HCID 178456191HCID 178456191, compound

Sources & evidence

ORD record
ord-372f6f103a624684887d59919156f23c
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (7/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes