Dimethylcarbamoyl Chloride → (5-(4-Chlorophenylsulfonyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridin-4-yl)methyl dimethylcarbamate

HRID 15765

Reaction equation

[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([N:11]2[CH2:16][CH2:15][C:14]3[NH:17][N:18]=[CH:19][C:13]=3[CH:12]2[CH2:20][OH:21])(=[O:10])=[O:9])=[CH:4][CH:3]=1.[CH3:22][N:23]([CH3:27])[C:24](Cl)=[O:25].ClC1C=CC(S(N2C(CC)CC3(OCCO3)CC2CO)(=O)=O)=CC=1>>[CH3:22][N:23]([CH3:27])[C:24](=[O:25])[O:21][CH2:20][CH:12]1[C:13]2[CH:19]=[N:18][NH:17][C:14]=2[CH2:15][CH2:16][N:11]1[S:8]([C:5]1[CH:4]=[CH:3][C:2]([Cl:1])=[CH:7][CH:6]=1)(=[O:9])=[O:10]

Participants

Reactant 3

HCID 6598Dimethylcarbamoyl Chloride

HCID 46884456(5-(4-chlorophenylsulfonyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridin-4-yl)methanol

HCID 59342380(8-(4-Chlorophenylsulfonyl)-9-ethyl-1,4-dioxa-8-azaspiro[4.5]decan-7-yl)methanol

Product 1

HCID 16730799(5-(4-Chlorophenylsulfonyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridin-4-yl)methyl dimethylcarbamate

Procedure

Prepared by treatment of (5-(4-chlorophenylsulfonyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridin-4-yl)methanol with dimethylcarbamyl chloride as described for compound 111 in Example 14.

Sources & evidence

ORD record: ord-f36e63dddc5a4ca780a01bff8d78ffd5
Source dataset: uspto-grants-2010_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07732609B2

Linked notes

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