Sulfanilamide → HCID 24889767, compound

HRID 912105Notes

Reaction equation

HRID 912105 reaction equation
ClC1C(CCCl)=C(C2C=CC=C(OC)C=2)N=C(N2CCOCC2)N=1.NC1C=CC(S(N)(=O)=O)=CC=1.C[O:37][C:38]1[CH:39]=[C:40]([C:44]2[C:45]3[CH2:58][CH2:57][N:56]([C:59]4[CH:64]=[CH:63][C:62]([S:65]([NH2:68])(=[O:67])=[O:66])=[CH:61][CH:60]=4)[C:46]=3[N:47]=[C:48]([N:50]3[CH2:55][CH2:54][O:53][CH2:52][CH2:51]3)[N:49]=2)[CH:41]=[CH:42][CH:43]=1>>[OH:37][C:38]1[CH:39]=[C:40]([C:44]2[C:45]3[CH2:58][CH2:57][N:56]([C:59]4[CH:64]=[CH:63][C:62]([S:65]([NH2:68])(=[O:67])=[O:66])=[CH:61][CH:60]=4)[C:46]=3[N:47]=[C:48]([N:50]3[CH2:55][CH2:54][O:53][CH2:52][CH2:51]3)[N:49]=2)[CH:41]=[CH:42][CH:43]=1

Participants

4

Procedure

In the same manner as Example 1-A-01, from 4-[4-chloro-5-(2-chloroethyl)-6-(3-methoxyphenyl)-pyrimidin-2-yl]-morpholine and 4-aminobenzene sulfonamide, 4-(3-methoxy-phenyl)-7-(4-aminosulfonylphenyl)-2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidine was obtained, and subsequently, further in the same manner as Example 1-A-09, the desired compound was obtained.

Sources & evidence

ORD record
ord-82c156ceafa1446e9eaf84cc9d51bfbe
Source dataset
uspto-grants-2011_09
Patent number
US08022205B2

Reaction notes

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