4-Chlorobutane-1-sulphonyl chloride → HCID 69357820, compound

HRID 852567Notes

Reaction equation

HRID 852567 reaction equation
[CH3:1][O:2][C:3](=[O:20])[C:4]1[CH:18]=[C:17]([NH2:19])[CH:16]=[C:6]([C:7]([N:9]([CH2:13][CH2:14][CH3:15])[CH2:10][CH2:11][CH3:12])=[O:8])[CH:5]=1.[Cl:21][CH2:22][CH2:23][CH2:24][CH2:25][S:26](Cl)(=[O:28])=[O:27]>>[CH3:1][O:2][C:3](=[O:20])[C:4]1[CH:18]=[C:17]([NH:19][S:26]([CH2:25][CH2:24][CH2:23][CH2:22][Cl:21])(=[O:28])=[O:27])[CH:16]=[C:6]([C:7]([N:9]([CH2:10][CH2:11][CH3:12])[CH2:13][CH2:14][CH3:15])=[O:8])[CH:5]=1

Participants

3

Reactant 2

HCID 742124-Chlorobutane-1-sulphonyl chlorideHCID 22593627Methyl 3-amino-5-[(dipropylamino)carbonyl]Benzoate

Product 1

HCID 69357820HCID 69357820, compound

Procedure

Description 92 was prepared in an analogous manner to Description 91 from 5-amino-N,N-dipropyl-isophthalamic acid methyl ester (D88) and 4-chloro-butane-1-sulfonyl chloride.

Sources & evidence

ORD record
ord-b1c31a62af534b8fb0c1cd3276d91ff5
Source dataset
uspto-grants-2007_08
Patent number
US07253198B2

Reaction notes

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