Hexylamine → HCID 178444758, compound

HRID 481965Notes

Reaction equation

HRID 481965 reaction equation
Cl[C:2]1[CH:20]=[N:19][C:5]2[NH:6][C:7]([NH:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])=[N:8][S:9](=[O:11])(=[O:10])[C:4]=2[CH:3]=1.ClC1C=NC2NC(N3C=CN=C3)=NS(=O)(=O)C=2C=1.C(N)CCCCC>>[CH2:13]([NH:12][C:7]1[NH:6][C:3]2[CH:2]=[CH:20][N:19]=[CH:5][C:4]=2[S:9](=[O:11])(=[O:10])[N:8]=1)[CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]

Participants

4

Reactant 3

HCID 8102HexylamineHCID 10564945HCID 10564945, compoundHCID 178444757HCID 178444757, compound

Product 1

HCID 178444758HCID 178444758, compound

Procedure

In a similar manner the following compound was prepared: 7--Chloro-3-hexylamino-4H- pyrido[2,3-e]-1,2,4-thiadiazine 1,1-dioxide; m.p. 176-179° C.; from 7-chloro-3-(imidazol-1-yl)-4H-pyrido[2,3-e]-1,2,4-thiadiazine 1,1-dioxide and hexylamine.(Compound 12).

Workup

  1. customIn a similar manner the following compound was prepared

Sources & evidence

ORD record
ord-189f448e29f34ed4b58b3c9836c053f9
Source dataset
uspto-grants-1998_08
Patent number
US05792764

Reaction notes

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