HCID 19892102, compound → HCID 19892085, compound

HRID 893303Notes

Reaction equation

HRID 893303 reaction equation
Cl[C:2]1C(NCCCCCCSC)=NC=NC=1CC.[Cl:19][C:20]1[C:21]([N:27]([C:38]([Cl:40])=[O:39])[CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][S:36][CH3:37])=[N:22][CH:23]=[N:24][C:25]=1[CH3:26].CSCCCCCCCCC1N=C(N)C2C(=CC=CC=2)N=1>>[Cl:19][C:20]1[C:21]([N:27]([C:38]([Cl:40])=[O:39])[CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][S:36][CH3:37])=[N:22][CH:23]=[N:24][C:25]=1[CH2:26][CH3:2]

Participants

4

Reactant 3

HCID 19892102HCID 19892102, compoundHCID 19892104HCID 19892104, compoundHCID 21658400HCID 21658400, compound

Product 1

HCID 19892085HCID 19892085, compound

Procedure

In the same manner as mentioned above, 5-chloro-N-(6-methylthiohexyl)-6-ethyl-4-pyrimidineamine, 5-chloro-N-chlorocarbonyl-N-(8-methylthiooctyl)-6-methyl-4-pyrimidineamine and N-chlorocarbonyl-N-(8-methylthiooctyl-4-quinazolineamine were synthesized.

Workup

  1. customwere synthesized

Sources & evidence

ORD record
ord-d2abefc6d82c4f6484d19681d57191e5
Source dataset
uspto-grants-1992_06
Patent number
US05124333

Reaction notes

Loading…