Hydrochloric Acid → HCID 57936206, compound

HRID 1434979Notes

Reaction equation

HRID 1434979 reaction equation
Cl[C:2]1[N:7]=[C:6](Cl)[CH:5]=[CH:4][N:3]=1.[S:9]1[C:13](B(O)O)=[CH:12][C:11]2[CH:17]=[CH:18][CH:19]=[CH:20][C:10]1=2.C(OC([N:28]1[CH2:36][CH2:35][CH:34]([NH2:37])[CH2:33][C:29]21[CH2:32][CH2:31][CH2:30]2)=O)(C)(C)C.Cl>O1CCOCC1>[CH2:30]1[C:29]2([CH2:33][CH:34]([NH:37][C:2]3[N:7]=[C:6]([C:13]4[S:9][C:10]5[CH:20]=[CH:19][CH:18]=[CH:17][C:11]=5[CH:12]=4)[CH:5]=[CH:4][N:3]=3)[CH2:35][CH2:36][NH:28]2)[CH2:32][CH2:31]1

Participants

6

Reactant 4

HCID 313Hydrochloric AcidHCID 2359Benzo(B)Thiophene-2-Boronic AcidHCID 775312,4-DichloropyrimidineHCID 162286758-amino-5-Azaspiro[3.5]nonane-5-carboxylic acid 1,1-dimethylethyl ester

Product 1

HCID 57936206HCID 57936206, compound

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent

Procedure

The racemic title compound was prepared analogous to Method A, starting from 2,4-dichloro-pyrimidine, benzo[b]thiophen-2-boronic acid and 8-Amino-5-aza-spiro[3.5]nonane-5-carboxylic acid tert-butyl ester followed by BOC-deprotection with 4N-HCl in dioxane.

Sources & evidence

ORD record
ord-d600a529d82f4661a017895547998651
Source dataset
uspto-grants-2009_11
Patent number
US07615562B2

Reaction notes

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